Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018380.3 | 1059 | Missense Mutation | GGC,TGC | G132C | NP_060850.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271762.1 | 1059 | Intron | NP_001258691.1 | ||
NM_001271763.1 | 1059 | Intron | NP_001258692.1 | ||
NM_017803.4 | 1059 | Intron | NP_060273.1 |