Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016449.3 | 476 | Intron | NP_057533.2 | ||
XM_011530206.1 | 476 | Intron | XP_011528508.1 | ||
XM_011530207.2 | 476 | Intron | XP_011528509.1 | ||
XM_011530208.2 | 476 | Intron | XP_011528510.1 | ||
XM_011530209.2 | 476 | Intron | XP_011528511.1 | ||
XM_011530210.2 | 476 | Intron | XP_011528512.1 | ||
XM_017028813.1 | 476 | Intron | XP_016884302.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020070.3 | 476 | Missense Mutation | CGC,TGC | R40C | NP_064455.1 |
NM_152855.2 | 476 | Missense Mutation | CGC,TGC | R40C | NP_690594.1 |
XM_011530169.2 | 476 | Missense Mutation | CGC,TGC | R40C | XP_011528471.1 |