| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012302.2 | 2274 | Missense Mutation | TCG,TTG | S730L | NP_001012302.2 |
| XM_011520048.1 | 2274 | Intron | XP_011518350.1 | ||
| XM_011520051.2 | 2274 | Intron | XP_011518353.1 | ||
| XM_011520052.2 | 2274 | Intron | XP_011518354.1 | ||
| XM_011520053.2 | 2274 | Missense Mutation | TCG,TTG | S431L | XP_011518355.1 |
| XM_017017644.1 | 2274 | Intron | XP_016873133.1 | ||
| XM_017017645.1 | 2274 | Intron | XP_016873134.1 | ||
| XM_017017646.1 | 2274 | Intron | XP_016873135.1 | ||
| XM_017017647.1 | 2274 | Intron | XP_016873136.1 |