| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015983.3 | 269 | Intron | NP_057067.1 | ||
| XM_006715734.3 | 269 | Intron | XP_006715797.1 | ||
| XM_011515420.2 | 269 | Missense Mutation | AGT,GGT | S47G | XP_011513722.1 |
| XM_011515422.2 | 269 | Intron | XP_011513724.1 | ||
| XM_011515423.2 | 269 | Intron | XP_011513725.1 | ||
| XM_017012292.1 | 269 | Missense Mutation | AGT,GGT | S47G | XP_016867781.1 |
| XM_017012293.1 | 269 | Missense Mutation | AGT,GGT | S47G | XP_016867782.1 |
| XM_017012294.1 | 269 | Missense Mutation | AGT,GGT | S47G | XP_016867783.1 |
| XM_017012295.1 | 269 | Intron | XP_016867784.1 |