| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_144970.2 | 667 | Missense Mutation | CAG,CGG | Q207R | NP_659407.1 |
| XM_005272589.2 | 667 | Missense Mutation | CAG,CGG | Q207R | XP_005272646.2 |
| XM_006724527.3 | 667 | Missense Mutation | CAG,CGG | Q207R | XP_006724590.2 |
| XM_006724528.2 | 667 | Missense Mutation | CAG,CGG | Q162R | XP_006724591.1 |
| XM_017029302.1 | 667 | Missense Mutation | CAG,CGG | Q218R | XP_016884791.1 |
| XM_017029303.1 | 667 | Missense Mutation | CAG,CGG | Q162R | XP_016884792.1 |
| XM_017029304.1 | 667 | Missense Mutation | CAG,CGG | Q88R | XP_016884793.1 |
| XM_017029305.1 | 667 | Missense Mutation | CAG,CGG | Q88R | XP_016884794.1 |