Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001105520.1 | 288 | Missense Mutation | TCC,TGC | S38C | NP_001098990.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016060.2 | 288 | Intron | NP_057144.1 | ||
XM_017024710.1 | 288 | Intron | XP_016880199.1 |