ID: 51156 | serpin family A member 10 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94280460..94293268, complement) | PZI, ZPI | 605271 |
ID: 319 | apolipoprotein F [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56360568..56362857, complement) | Apo-F, LTIP | 107760 |
ID: 259 | alpha-1-microglobulin/bikunin precursor [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114060127..114078300, complement) | A1M, EDC1, HCP, HI30, IATIL, ITI, ITIL, ITILC, UTI | 176870 |
ID: 3698 | inter-alpha-trypsin inhibitor heavy chain 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (7703316..7749520) | H2P, ITI-HC2, SHAP | 146640 |
ID: 54363 | hydroxyacid oxidase 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (7882985..7940458, complement) | GO, GOX, GOX1, HAOX1 | 605023 |
ID: 732 | complement C8 beta chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (56929207..56966015, complement) | C82 | 120960 |
ID: 325 | amyloid P component, serum [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (159587826..159588865) | HEL-S-92n, PTX2, SAP | 104770 |
ID: 336 | apolipoprotein A2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161222292..161223628, complement) | Apo-AII, ApoA-II, apoAII | 107670 |
ID: 2147 | coagulation factor II, thrombin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46719213..46739506) | PT, RPRGL2, THPH1 | 176930 |
ID: 3263 | hemopexin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6431049..6440987, complement) | HX | 142290 |
ID: 622 | 3-hydroxybutyrate dehydrogenase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197509783..197573343, complement) | BDH, SDR9C1 | 603063 |
ID: 763 | carbonic anhydrase 5A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87881549..87936529, complement) | CA5D, CAV, CAVA, GS1-21A4.1, CA5A | 114761 |
ID: 114770 | peptidoglycan recognition protein 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (15468645..15479501, complement) | HMFT0141, PGLYRPL, PGRP-L, PGRPL, TAGL-like, tagL, tagL-alpha, tagl-beta | 608199 |
ID: 284541 | cytochrome P450 family 4 subfamily A member 22 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (47137441..47149727) | | 615341 |
ID: 1369 | carboxypeptidase N subunit 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100042193..100081869, complement) | CPN, SCPN | 603103 |
ID: 3697 | inter-alpha-trypsin inhibitor heavy chain 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (52777599..52792068) | H1P, IATIH, IGHEP1, ITI-HC1, ITIH, SHAP | 147270 |
ID: 1 | alpha-1-B glycoprotein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (58345183..58353492, complement) | A1B, ABG, GAB, HYST2477 | 138670 |
ID: 140290 | t-complex 10 like [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (32573721..32585523, complement) | C21orf77, LINC00846, PRED77, TCP10A-1, TCP10A-2 | 608365 |
ID: 2267 | fibrinogen like 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17864389..17895538, complement) | HFREP1, HP-041, HPS, LFIRE-1, LFIRE1 | 605776 |
ID: 10400 | phosphatidylethanolamine N-methyltransferase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17505563..17592142, complement) | PEAMT, PEMPT2, PLMT, PNMT, PEMT | 602391 |