Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001288950.1 | 2167 | Missense Mutation | TGC,TTC | C633F | NP_001275879.1 |
NM_014065.3 | 2167 | Missense Mutation | TGC,TTC | C608F | NP_054784.2 |
XM_017006266.1 | 2167 | UTR 3 | XP_016861755.1 | ||
XM_017006267.1 | 2167 | UTR 3 | XP_016861756.1 | ||
XM_017006268.1 | 2167 | UTR 3 | XP_016861757.1 | ||
XM_017006269.1 | 2167 | UTR 3 | XP_016861758.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001485.2 | 2167 | Intron | NP_001001485.1 | ||
NM_001001486.1 | 2167 | Intron | NP_001001486.1 | ||
NM_001001487.1 | 2167 | Intron | NP_001001487.1 | ||
NM_001199179.1 | 2167 | Intron | NP_001186108.1 | ||
NM_001199180.1 | 2167 | Intron | NP_001186109.1 | ||
NM_001199181.1 | 2167 | Intron | NP_001186110.1 | ||
NM_001199182.1 | 2167 | Intron | NP_001186111.1 | ||
NM_001199183.1 | 2167 | Intron | NP_001186112.1 | ||
NM_001199184.1 | 2167 | Intron | NP_001186113.1 | ||
NM_001199185.1 | 2167 | Intron | NP_001186114.1 | ||
NM_014382.3 | 2167 | Intron | NP_055197.2 | ||
XM_005247354.2 | 2167 | Intron | XP_005247411.1 | ||
XM_005247355.2 | 2167 | Intron | XP_005247412.1 | ||
XM_005247356.2 | 2167 | Intron | XP_005247413.1 | ||
XM_005247358.2 | 2167 | Intron | XP_005247415.1 | ||
XM_011512686.2 | 2167 | Intron | XP_011510988.1 | ||
XM_017006164.1 | 2167 | Intron | XP_016861653.1 |