| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190463.1 | 466 | Intron | NP_001177392.1 | ||
| NM_001902.5 | 466 | Missense Mutation | AGT,GGT | S90G | NP_001893.2 |
| NM_153742.4 | 466 | Missense Mutation | AGT,GGT | S90G | NP_714964.2 |
| XM_005270509.3 | 466 | UTR 5 | XP_005270566.1 | ||
| XM_017000416.1 | 466 | Intron | XP_016855905.1 |