| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001007088.1 | 656 | Missense Mutation | CAT,CGT | H116R | NP_001007089.1 |
| NM_001178099.1 | 656 | Missense Mutation | CAT,CGT | H135R | NP_001171570.1 |
| NM_006962.1 | 656 | Missense Mutation | CAT,CGT | H135R | NP_008893.1 |