Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000124.3 | 764 | Intron | NP_000115.1 | ||
NM_001277058.1 | 764 | Missense Mutation | CGT,GGT | R638G | NP_001263987.1 |
NM_001277059.1 | 764 | Missense Mutation | CGT,GGT | R638G | NP_001263988.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_170753.3 | 764 | Missense Mutation | CGT,GGT | R170G | NP_736609.2 |