| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282382.1 | 553 | Missense Mutation | TTC,TTG | F50L | NP_001269311.1 |
| NM_001282383.1 | 553 | Missense Mutation | TTC,TTG | F50L | NP_001269312.1 |
| NM_004219.3 | 553 | Missense Mutation | TTC,TTG | F50L | NP_004210.1 |