| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024546.3 | 1736 | Missense Mutation | TTG,TTT | L559F | NP_078822.3 |
| XM_011535225.1 | 1736 | Missense Mutation | TTG,TTT | L482F | XP_011533527.1 |
| XM_017020743.1 | 1736 | Missense Mutation | TTG,TTT | L482F | XP_016876232.1 |