| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172557.1 | 2596 | Intron | NP_001166028.1 | ||
| NM_005895.3 | 2596 | Missense Mutation | AGC,GGC | S1478G | NP_005886.2 |
| XM_005266164.4 | 2596 | Missense Mutation | AGC,GGC | S1438G | XP_005266221.1 |
| XM_005266167.4 | 2596 | Missense Mutation | AGC,GGC | S1287G | XP_005266224.1 |
| XM_006719736.3 | 2596 | Missense Mutation | AGC,GGC | S1478G | XP_006719799.1 |
| XM_006719737.3 | 2596 | Missense Mutation | AGC,GGC | S1478G | XP_006719800.1 |
| XM_011534793.2 | 2596 | Missense Mutation | AGC,GGC | S1387G | XP_011533095.1 |
| XM_011534794.2 | 2596 | Missense Mutation | AGC,GGC | S830G | XP_011533096.1 |