Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001143980.1 | 2052 | Missense Mutation | CGC,TGC | R629C | NP_001137452.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_011522780.2 | 2052 | Intron | XP_011521082.1 |