Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198525.2 | 3861 | Missense Mutation | CGG,TGG | R1262W | NP_940927.2 |
XM_011521531.2 | 3861 | Missense Mutation | CGG,TGG | R1303W | XP_011519833.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308025.1 | 3861 | Intron | NP_001294954.1 | ||
NM_152259.3 | 3861 | Intron | NP_689472.3 |