| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271534.1 | 6469 | Missense Mutation | GCA,GGA | A1988G | NP_001258463.1 |
| NM_001389.3 | 6469 | Missense Mutation | GCA,GGA | A2006G | NP_001380.2 |
| XM_017028281.1 | 6469 | Missense Mutation | GCA,GGA | A1770G | XP_016883770.1 |