Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001290137.1 | 1184 | Missense Mutation | CCG,CGG | P230R | NP_001277066.1 |
NM_001290139.1 | 1184 | Missense Mutation | CCG,CGG | P230R | NP_001277068.1 |
NM_001323635.1 | 1184 | Missense Mutation | CCG,CGG | P230R | NP_001310564.1 |
NM_001323636.1 | 1184 | Silent Mutation | GCC,GCG | A203A | NP_001310565.1 |
NM_032304.3 | 1184 | Missense Mutation | CCG,CGG | P230R | NP_115680.1 |
XM_005255631.4 | 1184 | Intron | XP_005255688.1 | ||
XM_005255632.1 | 1184 | Missense Mutation | CCG,CGG | P221R | XP_005255689.1 |
XM_011522711.1 | 1184 | Intron | XP_011521013.1 | ||
XM_011522712.1 | 1184 | Missense Mutation | CCG,CGG | P229R | XP_011521014.1 |
XM_017023773.1 | 1184 | Intron | XP_016879262.1 | ||
XM_017023774.1 | 1184 | UTR 3 | XP_016879263.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304799.1 | 1184 | Intron | NP_001291728.1 | ||
NM_022493.2 | 1184 | Intron | NP_071938.1 |