| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281293.1 | 3577 | Missense Mutation | AGT,GGT | S689G | NP_001268222.1 |
| NM_001281294.1 | 3577 | Missense Mutation | AGT,GGT | S653G | NP_001268223.1 |
| NM_012482.4 | 3577 | Missense Mutation | AGT,GGT | S689G | NP_036614.1 |
| XM_017000887.1 | 3577 | Missense Mutation | AGT,GGT | S689G | XP_016856376.1 |
| XM_017000888.1 | 3577 | Missense Mutation | AGT,GGT | S689G | XP_016856377.1 |