| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020812.3 | 5646 | Missense Mutation | CGG,CTG | R1851L | NP_065863.2 |
| XM_005260000.2 | 5646 | Missense Mutation | CGG,CTG | R1917L | XP_005260057.1 |
| XM_005260001.2 | 5646 | Missense Mutation | CGG,CTG | R1886L | XP_005260058.1 |
| XM_006722804.3 | 5646 | Missense Mutation | CGG,CTG | R963L | XP_006722867.1 |
| XM_011528150.1 | 5646 | Missense Mutation | CGG,CTG | R1897L | XP_011526452.1 |
| XM_011528151.1 | 5646 | Missense Mutation | CGG,CTG | R1893L | XP_011526453.1 |
| XM_011528152.1 | 5646 | Missense Mutation | CGG,CTG | R1862L | XP_011526454.1 |