Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022336.3 | 1549 | Missense Mutation | CAG,CGG | Q420R | NP_071731.1 |
XM_006712204.1 | 1549 | Missense Mutation | CAG,CGG | Q452R | XP_006712267.1 |
XM_011510502.2 | 1549 | Missense Mutation | CAG,CGG | Q500R | XP_011508804.2 |
XM_011510503.2 | 1549 | Missense Mutation | CAG,CGG | Q468R | XP_011508805.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006267.4 | 1549 | Intron | NP_006258.3 | ||
XM_005264002.2 | 1549 | Intron | XP_005264059.1 | ||
XM_005264003.2 | 1549 | Intron | XP_005264060.1 | ||
XM_005264004.2 | 1549 | Intron | XP_005264061.1 | ||
XM_005264005.4 | 1549 | Intron | XP_005264062.1 | ||
XM_005264007.2 | 1549 | Intron | XP_005264064.1 | ||
XM_011511575.2 | 1549 | Intron | XP_011509877.1 | ||
XM_011511576.2 | 1549 | Intron | XP_011509878.1 | ||
XM_011511578.2 | 1549 | Intron | XP_011509880.1 | ||
XM_017004623.1 | 1549 | Intron | XP_016860112.1 | ||
XM_017004624.1 | 1549 | Intron | XP_016860113.1 | ||
XM_017004625.1 | 1549 | Intron | XP_016860114.1 |