Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005481.2 | 2733 | Missense Mutation | TCT,TGT | S861C | NP_005472.2 |
XM_017026120.1 | 2733 | Missense Mutation | TCT,TGT | S792C | XP_016881609.1 |
XM_017026121.1 | 2733 | Missense Mutation | TCT,TGT | S686C | XP_016881610.1 |