Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243768.1 | 692 | Missense Mutation | AGG,GGG | R101G | NP_001230697.1 |
NM_001270517.1 | 692 | UTR 3 | NP_001257446.1 | ||
NM_198544.3 | 692 | Missense Mutation | AGG,GGG | R122G | NP_940946.1 |
NM_199006.2 | 692 | UTR 3 | NP_950171.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302.4 | 692 | Missense Mutation | AGG,GGG | R63G | NP_001293.3 |