| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001128310.2 | 2222 | Missense Mutation | TTG,TTT | L664F | NP_001121782.1 |
| NM_001291976.1 | 2222 | Missense Mutation | TTG,TTT | L539F | NP_001278905.1 |
| NM_001291977.1 | 2222 | Missense Mutation | TTG,TTT | L539F | NP_001278906.1 |
| NM_004684.5 | 2222 | Missense Mutation | TTG,TTT | L664F | NP_004675.3 |