| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005879.2 | 766 | Missense Mutation | CAT,CGT | H311R | NP_005870.2 |
| XM_011533264.1 | 766 | Missense Mutation | CAT,CGT | H234R | XP_011531566.1 |
| XM_017005526.1 | 766 | Missense Mutation | CAT,CGT | H212R | XP_016861015.1 |