Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001184739.1 | 645 | Silent Mutation | CGC,CGT | R147R | NP_001171668.1 |
NM_001308067.1 | 645 | Intron | NP_001294996.1 | ||
NM_174944.3 | 645 | Intron | NP_777604.2 | ||
XM_011536663.2 | 645 | Silent Mutation | CGC,CGT | R71R | XP_011534965.1 |
XM_017021226.1 | 645 | Intron | XP_016876715.1 |