| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001322286.1 | 913 | Missense Mutation | AGT,GGT | S261G | NP_001309215.1 |
| NM_001322290.1 | 913 | Missense Mutation | AGT,GGT | S261G | NP_001309219.1 |
| NM_001322291.1 | 913 | Intron | NP_001309220.1 | ||
| NM_145756.2 | 913 | Missense Mutation | AGT,GGT | S261G | NP_665699.1 |
| XM_006722432.3 | 913 | Missense Mutation | AGT,GGT | S261G | XP_006722495.1 |
| XM_017025687.1 | 913 | Missense Mutation | AGT,GGT | S261G | XP_016881176.1 |
| XM_017025688.1 | 913 | Missense Mutation | AGT,GGT | S261G | XP_016881177.1 |
| XM_017025689.1 | 913 | Intron | XP_016881178.1 |