Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135050.1 | 3622 | Missense Mutation | CGT,TGT | R1142C | NP_001128522.1 |
NM_020789.3 | 3622 | Missense Mutation | CGT,TGT | R1126C | NP_065840.2 |
XM_017001884.1 | 3622 | Intron | XP_016857373.1 |