Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001203260.1 | 145 | Intron | NP_001190189.1 | ||
NM_001203261.1 | 145 | Intron | NP_001190190.1 | ||
NM_001203262.1 | 145 | Intron | NP_001190191.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003251.3 | 145 | Missense Mutation | CTG,GTG | L42V | NP_003242.1 |