| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_052853.3 | 813 | Missense Mutation | GCC,GTC | A137V | NP_443085.2 |
| XM_006716170.3 | 813 | Missense Mutation | GCC,GTC | A137V | XP_006716233.1 |
| XM_011516675.2 | 813 | Missense Mutation | GCC,GTC | A137V | XP_011514977.1 |