| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_144616.3 | 598 | Missense Mutation | AGC,GGC | S45G | NP_653217.1 |
| XM_017026285.1 | 598 | Missense Mutation | AGC,GGC | S91G | XP_016881774.1 |
| XM_017026286.1 | 598 | Missense Mutation | AGC,GGC | S91G | XP_016881775.1 |
| XM_017026287.1 | 598 | Missense Mutation | AGC,GGC | S45G | XP_016881776.1 |