Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145047.1 | 1013 | Missense Mutation | CCG,CTG | P305L | NP_001138519.1 |
NM_001145048.1 | 1013 | Missense Mutation | CCG,CTG | P238L | NP_001138520.1 |
NM_001145049.1 | 1013 | Missense Mutation | CCG,CTG | P222L | NP_001138521.1 |
NM_007266.3 | 1013 | Missense Mutation | CCG,CTG | P331L | NP_009197.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282729.1 | 1013 | Intron | NP_001269658.1 | ||
NM_001282730.1 | 1013 | Intron | NP_001269659.1 | ||
NM_001282731.1 | 1013 | Intron | NP_001269660.1 | ||
NM_001282732.1 | 1013 | Intron | NP_001269661.1 | ||
NM_014860.2 | 1013 | Intron | NP_055675.1 | ||
XM_005264672.4 | 1013 | Intron | XP_005264729.1 |