Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014234.4 | 111 | Missense Mutation | CTC,GTC | L27V | NP_055049.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077516.1 | 111 | Intron | NP_001070984.1 | ||
NM_001288777.1 | 111 | Intron | NP_001275706.1 | ||
NM_006979.2 | 111 | Intron | NP_008910.2 |