| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015284.3 | 176 | Missense Mutation | CAC,CGC | H31R | NP_056099.3 |
| XM_005270686.3 | 176 | Missense Mutation | CAC,CGC | H52R | XP_005270743.1 |
| XM_006710501.3 | 176 | Missense Mutation | CAC,CGC | H31R | XP_006710564.1 |
| XM_011541106.2 | 176 | Missense Mutation | CAC,CGC | H12R | XP_011539408.1 |
| XM_011541107.2 | 176 | Intron | XP_011539409.1 | ||
| XM_017000819.1 | 176 | Missense Mutation | CAC,CGC | H52R | XP_016856308.1 |
| XM_017000820.1 | 176 | Missense Mutation | CAC,CGC | H52R | XP_016856309.1 |
| XM_017000821.1 | 176 | Intron | XP_016856310.1 |