| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142703.1 | 569 | Missense Mutation | TCA,TTA | S79L | NP_001136175.1 |
| NM_001142704.1 | 569 | Missense Mutation | TCA,TTA | S79L | NP_001136176.1 |
| NM_198947.3 | 569 | Missense Mutation | TCA,TTA | S109L | NP_945185.1 |