Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001007072.1 | 673 | Intron | NP_001007073.1 | ||
NM_017894.5 | 673 | Intron | NP_060364.4 | ||
NM_181877.3 | 673 | Intron | NP_870992.2 | ||
XM_017022392.1 | 673 | Missense Mutation | CGT,TGT | R139C | XP_016877881.1 |
XM_017022393.1 | 673 | Missense Mutation | CGT,TGT | R139C | XP_016877882.1 |