Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182553.2 | 1040 | Intron | NP_872359.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001300861.1 | 1040 | Missense Mutation | CGG,TGG | R213W | NP_001287790.1 |
NM_020470.2 | 1040 | Missense Mutation | CGG,TGG | R265W | NP_065203.2 |
XM_005273720.3 | 1040 | Silent Mutation | CCC,CCT | P294P | XP_005273777.1 |
XM_017017139.1 | 1040 | Silent Mutation | CCC,CCT | P306P | XP_016872628.1 |
XM_017017140.1 | 1040 | Missense Mutation | CGG,TGG | R277W | XP_016872629.1 |
XM_017017141.1 | 1040 | Intron | XP_016872630.1 |