Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182553.2 | 986 | Intron | NP_872359.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001300861.1 | 986 | Missense Mutation | CGC,TGC | R195C | NP_001287790.1 |
NM_020470.2 | 986 | Missense Mutation | CGC,TGC | R247C | NP_065203.2 |
XM_005273720.3 | 986 | Silent Mutation | TGC,TGT | C276C | XP_005273777.1 |
XM_017017139.1 | 986 | Silent Mutation | TGC,TGT | C288C | XP_016872628.1 |
XM_017017140.1 | 986 | Missense Mutation | CGC,TGC | R259C | XP_016872629.1 |
XM_017017141.1 | 986 | Intron | XP_016872630.1 |