|
ENST00000245414.9:c.978G>T
MANE Select
|
ENSP00000245414.4:p.Ter326Tyr
|
|
|
ENST00000638452.2:c.-169+34262C>A
|
ENSP00000492349.2:n.-169+34262C>A
|
|
|
ENST00000638504.1:n.206+64011C>A
|
|
|
|
ENST00000638568.2:c.-311+34262C>A
|
ENSP00000491158.2:n.-311+34262C>A
|
|
|
ENST00000639899.1:n.289+34262C>A
|
|
|
|
ENST00000640655.2:c.-637-2241C>A
|
ENSP00000491596.2:n.-637-2241C>A
|
|
|
ENST00000679743.1:c.599G>T
|
ENSP00000505257.1:n.599G>T
|
|
|
ENST00000679786.1:n.130+2606G>T
|
|
|
|
ENST00000679921.1:c.292+2606G>T
|
ENSP00000505766.1:n.292+2606G>T
|
|
|
ENST00000679945.1:n.130+2606G>T
|
|
|
|
ENST00000679964.1:n.50+1716G>T
|
|
|
|
ENST00000680139.1:c.792G>T
|
ENSP00000506148.1:p.Ter264Tyr
|
|
|
ENST00000680380.1:n.136+411G>T
|
|
|
|
ENST00000680562.1:c.426G>T
|
ENSP00000505853.1:p.Ter142Tyr
|
|
|
ENST00000680594.1:n.136+411G>T
|
|
|
|
ENST00000680903.1:c.855G>T
|
ENSP00000505720.1:p.Ter285Tyr
|
|
|
ENST00000681049.1:n.50+1716G>T
|
|
|
|
ENST00000681240.1:c.228G>T
|
ENSP00000506034.1:p.Ter76Tyr
|
|
|
ENST00000681336.1:c.225G>T
|
ENSP00000505242.1:p.Ter75Tyr
|
|
|
ENST00000681595.1:c.539G>T
|
ENSP00000506023.1:n.539G>T
|
|
|
ENST00000681634.1:n.136+411G>T
|
|
|
|
ENST00000681694.1:c.290G>T
|
ENSP00000506552.1:n.290G>T
|
|
|
ENST00000681715.1:c.476G>T
|
ENSP00000506545.1:n.476G>T
|
|
|
ENST00000245414.8:c.978G>T
|
ENSP00000245414.4:p.Ter326Tyr
|
|
|
ENST00000405885.6:c.978G>T
|
ENSP00000384406.1:p.Ter326Tyr
|
|
|
ENST00000472045.1:n.4287G>T
|
|
|
|
NM_002198.2:c.978G>T
|
NP_002189.1:p.Ter326Tyr
|
|
|
XM_011543378.1:c.855G>T
|
XP_011541680.1:p.Ter285Tyr
|
|
|
XM_011543379.1:c.726G>T
|
XP_011541681.1:p.Ter242Tyr
|
|
|
XR_427711.2:n.1039G>T
|
|
|
|
NM_001354924.1:c.855G>T
|
NP_001341853.1:p.Ter285Tyr
|
|
|
NM_001354925.1:c.792G>T
|
NP_001341854.1:p.Ter264Tyr
|
|
|
NR_149068.1:n.1039G>T
|
|
|
|
XM_011543379.2:c.726G>T
|
XP_011541681.1:p.Ter242Tyr
|
|
|
NM_002198.3:c.978G>T
MANE Select
|
NP_002189.1:p.Ter326Tyr
|
|
