| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001297713.1 | 2891 | Missense Mutation | CAC,CGC | H618R | NP_001284642.1 |
| NM_015441.2 | 2891 | Missense Mutation | CAC,CGC | H617R | NP_056256.1 |
| XM_005245075.2 | 2891 | Missense Mutation | CAC,CGC | H619R | XP_005245132.1 |
| XM_011509398.2 | 2891 | Missense Mutation | CAC,CGC | H377R | XP_011507700.1 |
| XM_017000967.1 | 2891 | Intron | XP_016856456.1 |