| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304271.1 | 565 | Intron | NP_001291200.1 | ||
| NM_001304272.1 | 565 | Missense Mutation | TTG,TTT | L76F | NP_001291201.1 |
| NM_001304273.1 | 565 | Missense Mutation | TTG,TTT | L76F | NP_001291202.1 |
| NM_024585.3 | 565 | Missense Mutation | TTG,TTT | L76F | NP_078861.1 |