| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001202855.2 | 1536 | Missense Mutation | AGC,TGC | S477C | NP_001189784.1 |
| NM_017460.5 | 1536 | Missense Mutation | AGC,TGC | S478C | NP_059488.2 |
| XM_017011780.1 | 1536 | Intron | XP_016867269.1 |