Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002251.2 | 672 | Missense Mutation | CCG,CTG | P176L | NP_001002251.2 |
NM_001002252.2 | 672 | Missense Mutation | CCG,CTG | P176L | NP_001002252.2 |
NM_001278378.1 | 672 | Missense Mutation | CCG,CTG | P176L | NP_001265307.1 |
NM_001278379.1 | 672 | Intron | NP_001265308.1 | ||
NM_001278380.1 | 672 | UTR 5 | NP_001265309.1 | ||
NM_016638.3 | 672 | Missense Mutation | CCG,CTG | P176L | NP_057722.3 |
NM_018694.3 | 672 | Missense Mutation | CCG,CTG | P176L | NP_061164.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304833.1 | 672 | Intron | NP_001291762.1 | ||
NM_001304834.1 | 672 | Intron | NP_001291763.1 | ||
NM_001304835.1 | 672 | Intron | NP_001291764.1 | ||
NM_001304836.1 | 672 | Intron | NP_001291765.1 | ||
NM_001304837.1 | 672 | Intron | NP_001291766.1 | ||
NM_001304838.1 | 672 | Intron | NP_001291767.1 | ||
NM_024623.2 | 672 | Intron | NP_078899.1 |