Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099784.2 | 378 | Intron | NP_001093254.2 | ||
NM_001282351.1 | 378 | Intron | NP_001269280.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152288.2 | 378 | Missense Mutation | CGG,TGG | R58W | NP_689501.1 |