| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289160.1 | 494 | Missense Mutation | TCG,TTG | S118L | NP_001276089.1 |
| NM_001289161.1 | 494 | Intron | NP_001276090.1 | ||
| NM_005931.4 | 494 | Missense Mutation | TCG,TTG | S150L | NP_005922.2 |