Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001173531.2 | 1140 | UTR 5 | NP_001167002.1 | ||
NM_001285986.1 | 1140 | UTR 5 | NP_001272915.1 | ||
NM_001285987.1 | 1140 | Missense Mutation | GCT,GTT | A46V | NP_001272916.1 |
NM_002701.5 | 1140 | Intron | NP_002692.2 | ||
NM_203289.5 | 1140 | UTR 5 | NP_976034.4 |