| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001125.3 | 776 | Missense Mutation | ACA,GCA | T57A | NP_001116.1 |
| NM_001291949.1 | 776 | Missense Mutation | ACA,GCA | T57A | NP_001278878.1 |
| NM_001291950.1 | 776 | Intron | NP_001278879.1 | ||
| XM_011512438.2 | 776 | Missense Mutation | ACA,GCA | T57A | XP_011510740.1 |