Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198863.1 | 2956 | Intron | NP_001185792.1 | ||
NM_003915.5 | 2956 | Intron | NP_003906.2 | ||
NM_152925.2 | 2956 | Intron | NP_690902.1 | ||
NM_152926.2 | 2956 | Intron | NP_690903.1 | ||
NM_152927.2 | 2956 | Intron | NP_690904.1 | ||
NM_152928.2 | 2956 | Intron | NP_690905.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198838.1 | 2956 | Missense Mutation | ACG,ATG | T895M | NP_001185767.1 |
NM_001198840.1 | 2956 | Missense Mutation | ACG,ATG | T895M | NP_001185769.1 |
NM_006047.5 | 2956 | Missense Mutation | ACG,ATG | T895M | NP_006038.2 |
NM_152838.3 | 2956 | Missense Mutation | ACG,ATG | T895M | NP_690051.1 |