| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001260502.1 | 1842 | Missense Mutation | CTT,TTT | L565F | NP_001247431.1 |
| NM_001260503.1 | 1842 | Missense Mutation | CTT,TTT | L264F | NP_001247432.1 |
| NM_014230.3 | 1842 | Missense Mutation | CTT,TTT | L603F | NP_055045.2 |