Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001710.2 | 1718 | Missense Mutation | CTG,GTG | L251V | NP_001001710.1 |
XM_006717108.2 | 1718 | Missense Mutation | CTG,GTG | L235V | XP_006717171.2 |
XM_011518694.1 | 1718 | Missense Mutation | CTG,GTG | L286V | XP_011516996.1 |
XM_011518695.1 | 1718 | Missense Mutation | CTG,GTG | L248V | XP_011516997.1 |
XM_011518696.2 | 1718 | Intron | XP_011516998.1 | ||
XM_011518697.1 | 1718 | Missense Mutation | CCT,CGT | P254R | XP_011516999.1 |
XM_017014718.1 | 1718 | Missense Mutation | CTG,GTG | L164V | XP_016870207.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006088.5 | 1718 | Intron | NP_006079.1 |