| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000743.4 | 1586 | Intron | NP_000734.2 | ||
| NM_001166694.1 | 1586 | Intron | NP_001160166.1 | ||
| XM_006720382.2 | 1586 | Intron | XP_006720445.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000745.3 | 1586 | Missense Mutation | CAA,CAT | Q462H | NP_000736.2 |
| NM_001307945.1 | 1586 | UTR 3 | NP_001294874.1 | ||
| XM_005254142.3 | 1586 | UTR 3 | XP_005254199.1 | ||
| XM_017021881.1 | 1586 | UTR 3 | XP_016877370.1 |