| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281710.1 | 76 | Intron | NP_001268639.1 | ||
| NM_001281711.1 | 76 | Intron | NP_001268640.1 | ||
| NM_001281712.1 | 76 | Intron | NP_001268641.1 | ||
| NM_015341.4 | 76 | Missense Mutation | TCT,TTT | S16F | NP_056156.2 |
| XM_005263908.3 | 76 | Missense Mutation | TCT,TTT | S16F | XP_005263965.1 |
| XM_006712388.3 | 76 | Missense Mutation | TCT,TTT | S16F | XP_006712451.1 |