Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001890.2 | 1384 | Silent Mutation | CCC,CCG | P436P | NP_001001890.1 |
NM_001122607.1 | 1384 | Intron | NP_001116079.1 | ||
NM_001754.4 | 1384 | Silent Mutation | CCC,CCG | P463P | NP_001745.2 |
XM_005261068.3 | 1384 | Silent Mutation | CCC,CCG | P451P | XP_005261125.1 |
XM_005261069.4 | 1384 | Silent Mutation | CCC,CCG | P399P | XP_005261126.1 |
XM_011529766.2 | 1384 | Silent Mutation | CCC,CCG | P463P | XP_011528068.1 |
XM_011529767.2 | 1384 | Silent Mutation | CCC,CCG | P450P | XP_011528069.1 |
XM_011529768.2 | 1384 | Silent Mutation | CCC,CCG | P386P | XP_011528070.1 |
XM_011529770.2 | 1384 | Intron | XP_011528072.1 | ||
XM_017028487.1 | 1384 | Silent Mutation | CCC,CCG | P412P | XP_016883976.1 |