Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006186.3 | 3701 | Missense Mutation | CTG,GTG | L524V | NP_006177.1 |
XM_005246621.3 | 3701 | Missense Mutation | CTG,GTG | L535V | XP_005246678.1 |
XM_005246622.3 | 3701 | Missense Mutation | CTG,GTG | L461V | XP_005246679.1 |
XM_006712553.3 | 3701 | Missense Mutation | CTG,GTG | L510V | XP_006712616.1 |
XM_011511246.1 | 3701 | Missense Mutation | ACT,AGT | T500S | XP_011509548.1 |
XM_017004219.1 | 3701 | Missense Mutation | CTG,GTG | L524V | XP_016859708.1 |
XM_017004220.1 | 3701 | Missense Mutation | CTG,GTG | L499V | XP_016859709.1 |