Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286356.1 | 262 | Missense Mutation | TCT,TTT | S51F | NP_001273285.1 |
NM_001286357.1 | 262 | Missense Mutation | TCT,TTT | S51F | NP_001273286.1 |
NM_001286358.1 | 262 | Missense Mutation | TCT,TTT | S51F | NP_001273287.1 |
NM_001286359.1 | 262 | Missense Mutation | TCT,TTT | S51F | NP_001273288.1 |
NM_002762.3 | 262 | Missense Mutation | TCT,TTT | S51F | NP_002753.2 |