Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282175.1 | 139 | Missense Mutation | AGG,GGG | R18G | NP_001269104.1 |
NM_001282176.1 | 139 | UTR 5 | NP_001269105.1 | ||
NM_001294.3 | 139 | Missense Mutation | AGG,GGG | R32G | NP_001285.1 |