Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001160305.2 | 633 | Silent Mutation | CTG,GTG | L216V | NP_001153777.1 |
NM_024860.3 | 633 | Silent Mutation | CTG,GTG | L192V | NP_079136.2 |
XM_011523336.1 | 633 | Missense Mutation | CTG,GTG | L216V | XP_011521638.1 |