Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003712.3 | 802 | Missense Mutation | CTG,GTG | L235V | NP_003703.1 |
NM_177526.2 | 802 | Missense Mutation | CTG,GTG | L179V | NP_803545.1 |
NM_177543.2 | 802 | Missense Mutation | CTG,GTG | L256V | NP_808211.1 |
XM_011528396.2 | 802 | Missense Mutation | CTG,GTG | L241V | XP_011526698.1 |