Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304833.1 | 708 | Missense Mutation | CGG,TGG | R141W | NP_001291762.1 |
NM_001304834.1 | 708 | UTR 5 | NP_001291763.1 | ||
NM_001304835.1 | 708 | UTR 5 | NP_001291764.1 | ||
NM_001304836.1 | 708 | UTR 5 | NP_001291765.1 | ||
NM_001304837.1 | 708 | UTR 5 | NP_001291766.1 | ||
NM_001304838.1 | 708 | UTR 5 | NP_001291767.1 | ||
NM_024623.2 | 708 | Missense Mutation | CGG,TGG | R81W | NP_078899.1 |