| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015048.1 | 1625 | Missense Mutation | TCG,TTG | S487L | NP_055863.1 |
| XM_005253858.4 | 1625 | Missense Mutation | TCG,TTG | S487L | XP_005253915.1 |
| XM_006719296.3 | 1625 | Missense Mutation | TCG,TTG | S487L | XP_006719359.1 |