Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098510.1 | 437 | Missense Mutation | TCC,TGC | S145C | NP_001091980.1 |
NM_001243135.1 | 437 | Missense Mutation | TCC,TGC | S106C | NP_001230064.1 |
NM_001243136.1 | 437 | Missense Mutation | TCC,TGC | S62C | NP_001230065.1 |
NM_145065.2 | 437 | Missense Mutation | TCC,TGC | S169C | NP_659502.2 |
XM_011544884.2 | 437 | Missense Mutation | TCC,TGC | S169C | XP_011543186.1 |
XM_017017465.1 | 437 | Missense Mutation | TCC,TGC | S20C | XP_016872954.1 |