| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014585.5 | 1814 | Missense Mutation | CCG,CTG | P443L | NP_055400.1 |
| XM_005246505.1 | 1814 | Missense Mutation | CCG,CTG | P403L | XP_005246562.1 |
| XM_017003938.1 | 1814 | Missense Mutation | CCG,CTG | P403L | XP_016859427.1 |