| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000959.3 | 352 | Missense Mutation | TCC,TTC | S29F | NP_000950.1 |
| NM_001039585.1 | 352 | Missense Mutation | TCC,TTC | S29F | NP_001034674.1 |
| XM_017001873.1 | 352 | Missense Mutation | TCC,TTC | S29F | XP_016857362.1 |