| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098540.2 | 1312 | Missense Mutation | TCA,TTA | S466L | NP_001092010.1 |
| NM_001166498.2 | 1312 | Missense Mutation | TCA,TTA | S392L | NP_001159970.1 |
| NM_001199830.1 | 1312 | Missense Mutation | TCA,TTA | S408L | NP_001186759.1 |
| NM_006665.5 | 1312 | Missense Mutation | TCA,TTA | S466L | NP_006656.2 |