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ENST00000245414.9:c.908_909delinsTT
MANE Select
|
ENSP00000245414.4:p.Ala303Val
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|
|
ENST00000638452.2:c.-169+34331_-169+34332delinsAA
|
ENSP00000492349.2:n.-169+34331_-169+34332delinsAA
|
|
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ENST00000638504.1:n.206+64080_206+64081delinsAA
|
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|
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ENST00000638568.2:c.-311+34331_-311+34332delinsAA
|
ENSP00000491158.2:n.-311+34331_-311+34332delinsAA
|
|
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ENST00000639899.1:n.289+34331_289+34332delinsAA
|
|
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ENST00000640655.2:c.-637-2172_-637-2171delinsAA
|
ENSP00000491596.2:n.-637-2172_-637-2171delinsAA
|
|
|
ENST00000679743.1:c.529_530delinsTT
|
ENSP00000505257.1:n.529_530delinsTT
|
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|
ENST00000679786.1:n.130+2536_130+2537delinsTT
|
|
|
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ENST00000679860.1:c.196_197delinsTT
|
|
|
|
ENST00000679921.1:c.292+2536_292+2537delinsTT
|
ENSP00000505766.1:n.292+2536_292+2537delinsTT
|
|
|
ENST00000679945.1:n.130+2536_130+2537delinsTT
|
|
|
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ENST00000679964.1:n.50+1646_50+1647delinsTT
|
|
|
|
ENST00000680139.1:c.722_723delinsTT
|
ENSP00000506148.1:p.Ala241Val
|
|
|
ENST00000680380.1:n.136+341_136+342delinsTT
|
|
|
|
ENST00000680562.1:c.356_357delinsTT
|
ENSP00000505853.1:p.Ala119Val
|
|
|
ENST00000680594.1:n.136+341_136+342delinsTT
|
|
|
|
ENST00000680903.1:c.785_786delinsTT
|
ENSP00000505720.1:p.Ala262Val
|
|
|
ENST00000681049.1:n.50+1646_50+1647delinsTT
|
|
|
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ENST00000681240.1:c.158_159delinsTT
|
ENSP00000506034.1:p.Ala53Val
|
|
|
ENST00000681336.1:c.155_156delinsTT
|
ENSP00000505242.1:p.Ala52Val
|
|
|
ENST00000681462.1:c.745_746delinsTT
|
|
|
|
ENST00000681595.1:c.469_470delinsTT
|
ENSP00000506023.1:n.469_470delinsTT
|
|
|
ENST00000681634.1:n.136+341_136+342delinsTT
|
|
|
|
ENST00000681694.1:c.220_221delinsTT
|
ENSP00000506552.1:n.220_221delinsTT
|
|
|
ENST00000681715.1:c.406_407delinsTT
|
ENSP00000506545.1:n.406_407delinsTT
|
|
|
ENST00000245414.8:c.908_909delinsTT
|
ENSP00000245414.4:p.Ala303Val
|
|
|
ENST00000405885.6:c.908_909delinsTT
|
ENSP00000384406.1:p.Ala303Val
|
|
|
ENST00000472045.1:n.4217_4218delinsTT
|
|
|
|
NM_002198.2:c.908_909delinsTT
|
NP_002189.1:p.Ala303Val
|
|
|
XM_011543378.1:c.785_786delinsTT
|
XP_011541680.1:p.Ala262Val
|
|
|
XM_011543379.1:c.656_657delinsTT
|
XP_011541681.1:p.Ala219Val
|
|
|
XR_427711.2:n.969_970delinsTT
|
|
|
|
NM_001354924.1:c.785_786delinsTT
|
NP_001341853.1:p.Ala262Val
|
|
|
NM_001354925.1:c.722_723delinsTT
|
NP_001341854.1:p.Ala241Val
|
|
|
NR_149068.1:n.969_970delinsTT
|
|
|
|
XM_011543379.2:c.656_657delinsTT
|
XP_011541681.1:p.Ala219Val
|
|
|
NM_002198.3:c.908_909delinsTT
MANE Select
|
NP_002189.1:p.Ala303Val
|
|
