Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012631.1 | 138 | Intron | NP_001012649.1 | ||
NM_001012632.1 | 138 | Intron | NP_001012650.1 | ||
NM_001012633.1 | 138 | Intron | NP_001012651.1 | ||
NM_001012634.1 | 138 | Intron | NP_001012652.1 | ||
NM_001012635.1 | 138 | Intron | NP_001012653.1 | ||
NM_001012636.1 | 138 | Intron | NP_001012654.1 | ||
NM_001012718.1 | 138 | Intron | NP_001012736.1 | ||
NM_001308078.1 | 138 | Missense Mutation | CTC,TTC | L22F | NP_001295007.1 |
NM_004221.4 | 138 | Intron | NP_004212.4 |