Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286746.1 | 452 | Missense Mutation | ATT,GTT | I135V | NP_001273675.1 |
NM_001286747.1 | 452 | Intron | NP_001273676.1 | ||
NM_024808.3 | 452 | Missense Mutation | ATT,GTT | I120V | NP_079084.3 |
XM_006719868.3 | 452 | Intron | XP_006719931.2 |