Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008703.2 | 871 | Missense Mutation | CTC,TTC | L100F | NP_001008703.1 |
NM_001008704.2 | 871 | Missense Mutation | CTC,TTC | L100F | NP_001008704.1 |
NM_001287396.1 | 871 | Missense Mutation | CTC,TTC | L100F | NP_001274325.1 |
NM_001287397.1 | 871 | Missense Mutation | CTC,TTC | L80F | NP_001274326.1 |
NM_001287398.1 | 871 | Missense Mutation | CTC,TTC | L80F | NP_001274327.1 |
NM_178508.4 | 871 | Missense Mutation | CTC,TTC | L100F | NP_848603.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001319077.1 | 871 | Intron | NP_001306006.1 | ||
NM_001319078.1 | 871 | Intron | NP_001306007.1 | ||
NM_001319079.1 | 871 | Intron | NP_001306008.1 | ||
NM_001319080.1 | 871 | Intron | NP_001306009.1 | ||
NM_001319081.1 | 871 | Intron | NP_001306010.1 | ||
NM_001319082.1 | 871 | Intron | NP_001306011.1 | ||
NM_002131.3 | 871 | Intron | NP_002122.1 | ||
NM_145899.2 | 871 | Intron | NP_665906.1 | ||
NM_145901.2 | 871 | Intron | NP_665908.1 | ||
NM_145902.2 | 871 | Intron | NP_665909.1 | ||
NM_145903.2 | 871 | Intron | NP_665910.1 | ||
NM_145905.2 | 871 | Intron | NP_665912.1 |