Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282606.1 | 751 | Missense Mutation | TTG,TTT | L210F | NP_001269535.1 |
NM_001282609.1 | 751 | Intron | NP_001269538.1 | ||
NM_001282610.1 | 751 | Missense Mutation | TTG,TTT | L132F | NP_001269539.1 |
NM_016056.3 | 751 | Missense Mutation | TTG,TTT | L163F | NP_057140.2 |