Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001170795.1 | 567 | Missense Mutation | CTC,TTC | L77F | NP_001164266.1 |
NM_016085.4 | 567 | Missense Mutation | CTC,TTC | L19F | NP_057169.2 |
NM_080592.3 | 567 | Missense Mutation | CTC,TTC | L132F | NP_542159.3 |