Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099218.2 | 2852 | Missense Mutation | TCT,TTT | S943F | NP_001092688.1 |
NM_001321233.1 | 2852 | Missense Mutation | TCT,TTT | S934F | NP_001308162.1 |
XM_011533084.1 | 2852 | Missense Mutation | TCT,TTT | S943F | XP_011531386.1 |