Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001007255.2 | 946 | Missense Mutation | CGG,TGG | R274W | NP_001007256.1 |
NM_152366.4 | 946 | Silent Mutation | GTC,GTT | V267V | NP_689579.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012394.3 | 946 | Intron | NP_036526.2 | ||
XM_011509624.2 | 946 | Intron | XP_011507926.1 |