Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000582.2 | 311 | Missense Mutation | TCT,TGT | S49C | NP_000573.1 |
NM_001040058.1 | 311 | Missense Mutation | TCT,TGT | S49C | NP_001035147.1 |
NM_001040060.1 | 311 | Intron | NP_001035149.1 | ||
NM_001251829.1 | 311 | Intron | NP_001238758.1 | ||
NM_001251830.1 | 311 | Missense Mutation | TCT,TGT | S62C | NP_001238759.1 |
XM_017008564.1 | 311 | Missense Mutation | TCT,TGT | S62C | XP_016864053.1 |