Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152755.1 | 419 | Missense Mutation | CGC,TGC | R106C | NP_689968.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001190415.1 | 419 | Intron | NP_001177344.1 | ||
NM_005641.3 | 419 | Intron | NP_005632.1 | ||
NM_139315.2 | 419 | Intron | NP_647476.1 |