| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014598.3 | 1008 | Missense Mutation | TCT,TTT | S296F | NP_055413.1 |
| XM_017024551.1 | 1008 | Missense Mutation | TCT,TTT | S360F | XP_016880040.1 |
| XM_017024552.1 | 1008 | Intron | XP_016880041.1 |