Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001242374.1 | 877 | Missense Mutation | TCT,TTT | S49F | NP_001229303.1 |
NM_001242375.1 | 877 | Missense Mutation | TCT,TTT | S49F | NP_001229304.1 |
NM_015391.3 | 877 | Intron | NP_056206.1 |