| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001162499.1 | 276 | Missense Mutation | TCC,TTC | S38F | NP_001155971.1 |
| NM_012298.2 | 276 | Missense Mutation | TCC,TTC | S38F | NP_036430.1 |
| XM_011533503.2 | 276 | Missense Mutation | TCC,TTC | S38F | XP_011531805.1 |
| XM_011533504.2 | 276 | Missense Mutation | TCC,TTC | S14F | XP_011531806.1 |