| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317338.1 | 293 | Missense Mutation | GCT,TCT | A3S | NP_001304267.1 |
| NM_017898.4 | 293 | Missense Mutation | GCT,TCT | A3S | NP_060368.2 |
| XM_006711407.2 | 293 | Intron | XP_006711470.1 | ||
| XM_011509684.1 | 293 | Intron | XP_011507986.1 | ||
| XM_017001581.1 | 293 | Missense Mutation | GCT,TCT | A3S | XP_016857070.1 |