Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020748.2 | 3268 | Missense Mutation | TCT,TGT | S1062C | NP_065799.1 |
XM_006721987.3 | 3268 | Missense Mutation | TCT,TGT | S1054C | XP_006722050.1 |
XM_011525058.2 | 3268 | Missense Mutation | TCT,TGT | S1054C | XP_011523360.1 |