Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164277.1 | 1444 | Intron | NP_001157749.1 | ||
NM_001164278.1 | 1444 | Missense Mutation | CTG,GTG | L335V | NP_001157750.1 |
NM_001164279.1 | 1444 | Intron | NP_001157751.1 | ||
NM_001164280.1 | 1444 | Intron | NP_001157752.1 | ||
NM_001467.5 | 1444 | Intron | NP_001458.1 |