Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000532.4 | 190 | Missense Mutation | CTG,GTG | L47V | NP_000523.2 |
NM_001178014.1 | 190 | Missense Mutation | CTG,GTG | L47V | NP_001171485.1 |
XM_011512873.1 | 190 | Missense Mutation | CTG,GTG | L47V | XP_011511175.1 |