|
ENST00000646891.2:c.2264T>G
MANE Select
|
ENSP00000493543.1:p.Ile755Ser
|
|
|
ENST00000288602.11:c.2384T>G
|
ENSP00000288602.7:p.Ile795Ser
|
|
|
ENST00000479537.6:c.1016T>G
|
|
|
|
ENST00000496384.7:c.2264T>G
|
ENSP00000419060.2:p.Ile755Ser
|
|
|
ENST00000497784.2:c.*1714T>G
|
ENSP00000420119.2:n.*1714T>G
|
|
|
ENST00000642228.1:c.*1342T>G
|
ENSP00000493678.1:n.*1342T>G
|
|
|
ENST00000642875.1:n.1662T>G
|
|
|
|
ENST00000644120.1:n.2517+5178T>G
|
|
|
|
ENST00000644650.1:c.1563T>G
|
|
|
|
ENST00000644905.1:n.3146T>G
|
|
|
|
ENST00000644969.2:c.2384T>G
MANE Plus Clinical
|
ENSP00000496776.1:p.Ile795Ser
|
|
|
ENST00000645443.1:n.2043T>G
|
|
|
|
ENST00000646730.1:c.*922T>G
|
ENSP00000494784.1:n.*922T>G
|
|
|
ENST00000646891.1:c.2264T>G
|
ENSP00000493543.1:p.Ile755Ser
|
|
|
ENST00000647434.1:c.1141T>G
|
ENSP00000495132.1:n.1141T>G
|
|
|
ENST00000288602.10:c.2264T>G
|
ENSP00000288602.6:p.Ile755Ser
|
|
|
ENST00000479537.5:c.630T>G
|
ENSP00000418033.1:n.630T>G
|
|
|
ENST00000496384.6:c.1087T>G
|
|
|
|
ENST00000497784.1:c.2299T>G
|
ENSP00000420119.1:n.2299T>G
|
|
|
NM_004333.4:c.2264T>G , LRG_299t1:c.2264T>G
|
NP_004324.2:p.Ile755Ser
|
|
|
XM_005250045.1:c.2264T>G
|
XP_005250102.1:p.Ile755Ser
|
|
|
XM_005250046.1:c.2127+5178T>G
|
XP_005250103.1:n.2127+5178T>G
|
|
|
XM_011516529.1:c.2127+5178T>G
|
XP_011514831.1:n.2127+5178T>G
|
|
|
XR_242190.1:n.2354T>G
|
|
|
|
XR_927520.1:n.2393T>G
|
|
|
|
XR_927521.1:n.2475T>G
|
|
|
|
XR_927522.1:n.2106T>G
|
|
|
|
XR_927523.1:n.2188T>G
|
|
|
|
NM_001354609.1:c.2264T>G
|
NP_001341538.1:p.Ile755Ser
|
|
|
NM_004333.5:c.2264T>G
|
NP_004324.2:p.Ile755Ser
|
|
|
NR_148928.1:n.3362T>G
|
|
|
|
XM_017012558.1:c.2384T>G
|
XP_016868047.1:p.Ile795Ser
|
|
|
XM_017012559.1:c.2247+5178T>G
|
XP_016868048.1:n.2247+5178T>G
|
|
|
XR_001744857.1:n.2474T>G
|
|
|
|
XR_001744858.1:n.2226T>G
|
|
|
|
NM_001354609.2:c.2264T>G
|
NP_001341538.1:p.Ile755Ser
|
|
|
NM_001374244.1:c.2384T>G
|
NP_001361173.1:p.Ile795Ser
|
|
|
NM_001374258.1:c.2384T>G
MANE Plus Clinical
|
NP_001361187.1:p.Ile795Ser
|
|
|
NM_004333.6:c.2264T>G
MANE Select
|
NP_004324.2:p.Ile755Ser
|
|
|
NM_001378467.1:c.2273T>G
|
NP_001365396.1:p.Ile758Ser
|
|
|
NM_001378468.1:c.2127+5178T>G
|
NP_001365397.1:n.2127+5178T>G
|
|
|
NM_001378469.1:c.2198T>G
|
NP_001365398.1:p.Ile733Ser
|
|
|
NM_001378470.1:c.2162T>G
|
NP_001365399.1:p.Ile721Ser
|
|
|
NM_001378471.1:c.2153T>G
|
NP_001365400.1:p.Ile718Ser
|
|
|
NM_001378472.1:c.2108T>G
|
NP_001365401.1:p.Ile703Ser
|
|
|
NM_001378473.1:c.2108T>G
|
NP_001365402.1:p.Ile703Ser
|
|
|
NM_001378474.1:c.2127+5178T>G
|
NP_001365403.1:n.2127+5178T>G
|
|
|
NM_001378475.1:c.2000T>G
|
NP_001365404.1:p.Ile667Ser
|
|
