Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001206942.1 | 1782 | Intron | NP_001193871.1 | ||
NM_001206943.1 | 1782 | Missense Mutation | ATT,GTT | I510V | NP_001193872.1 |
NM_001206944.1 | 1782 | Intron | NP_001193873.1 | ||
NM_001206945.1 | 1782 | Missense Mutation | ATT,GTT | I372V | NP_001193874.1 |
NM_006574.3 | 1782 | Intron | NP_006565.2 |