Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001167865.1 | 961 | Missense Mutation | CGT,TGT | R300C | NP_001161337.1 |
NM_017615.2 | 961 | Missense Mutation | CGT,TGT | R300C | NP_060085.2 |
XM_005269929.4 | 961 | Missense Mutation | CGT,TGT | R141C | XP_005269986.1 |
XM_005269930.3 | 961 | Missense Mutation | CGT,TGT | R141C | XP_005269987.1 |
XM_011539910.2 | 961 | Missense Mutation | CGT,TGT | R141C | XP_011538212.1 |
XM_017016359.1 | 961 | Missense Mutation | CGT,TGT | R141C | XP_016871848.1 |