| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193528.1 | 1214 | Missense Mutation | TCT,TTT | S33F | NP_001180457.1 |
| NM_024583.4 | 1214 | Missense Mutation | TCT,TTT | S40F | NP_078859.2 |
| XM_005246853.2 | 1214 | Missense Mutation | TCT,TTT | S60F | XP_005246910.1 |
| XM_005246854.4 | 1214 | Missense Mutation | TCT,TTT | S40F | XP_005246911.1 |
| XM_005246855.2 | 1214 | Missense Mutation | TCT,TTT | S40F | XP_005246912.1 |
| XM_005246856.2 | 1214 | Missense Mutation | TCT,TTT | S40F | XP_005246913.1 |
| XM_005246857.2 | 1214 | Missense Mutation | TCT,TTT | S40F | XP_005246914.1 |
| XM_011511839.2 | 1214 | Intron | XP_011510141.1 | ||
| XM_017004909.1 | 1214 | Missense Mutation | TCT,TTT | S40F | XP_016860398.1 |
| XM_017004910.1 | 1214 | Missense Mutation | TCT,TTT | S40F | XP_016860399.1 |