ENST00000700029.2:c.913_915delinsCAA
|
ENSP00000514759.2:p.Trp305Gln
|
|
ENST00000710265.1:c.820_822delinsCAA
|
ENSP00000518161.1:p.Trp274Gln
|
|
ENST00000472832.3:c.820_822delinsCAA
|
ENSP00000483066.2:p.Trp274Gln
|
|
ENST00000688158.2:n.1555_1557delinsCAA
|
|
|
ENST00000688922.2:c.*650_*652delinsCAA
|
ENSP00000508742.2:n.*650_*652delinsCAA
|
|
ENST00000700021.1:c.775_777delinsCAA
|
ENSP00000514757.1:p.Trp259Gln
|
|
ENST00000700022.1:c.*159_*161delinsCAA
|
ENSP00000514758.1:n.*159_*161delinsCAA
|
|
ENST00000700023.1:n.1978_1980delinsCAA
|
|
|
ENST00000700024.1:n.2212_2214delinsCAA
|
|
|
ENST00000700025.1:n.1589_1591delinsCAA
|
|
|
ENST00000700026.1:n.457_459delinsCAA
|
|
|
ENST00000700029.1:c.747_749delinsCAA
|
|
|
ENST00000706954.1:c.820_822delinsCAA
|
ENSP00000516674.1:p.Trp274Gln
|
|
ENST00000706955.1:c.*855_*857delinsCAA
|
ENSP00000516675.1:n.*855_*857delinsCAA
|
|
ENST00000686459.1:c.*406_*408delinsCAA
|
ENSP00000508909.1:n.*406_*408delinsCAA
|
|
ENST00000688158.1:c.*931_*933delinsCAA
|
ENSP00000509254.1:n.*931_*933delinsCAA
|
|
ENST00000688308.1:c.820_822delinsCAA
|
ENSP00000508752.1:p.Trp274Gln
|
|
ENST00000688922.1:c.741_743delinsCAA
|
|
|
ENST00000693560.1:c.1339_1341delinsCAA
|
ENSP00000509861.1:p.Trp447Gln
|
|
ENST00000371953.8:c.820_822delinsCAA
MANE Select
|
ENSP00000361021.3:p.Trp274Gln
|
|
ENST00000371953.7:c.820_822delinsCAA
|
ENSP00000361021.3:p.Trp274Gln
|
|
ENST00000472832.2:c.247_249delinsCAA
|
ENSP00000483066.1:p.Trp83Gln
|
|
NM_000314.5:c.820_822delinsCAA
|
NP_000305.3:p.Trp274Gln
|
|
NM_000314.6:c.820_822delinsCAA
|
NP_000305.3:p.Trp274Gln
|
|
NM_001304717.2:c.1339_1341delinsCAA
|
NP_001291646.2:p.Trp447Gln
|
|
NM_001304718.1:c.229_231delinsCAA
|
NP_001291647.1:p.Trp77Gln
|
|
XM_006717926.2:c.775_777delinsCAA
|
XP_006717989.1:p.Trp259Gln
|
|
XM_011539981.1:c.820_822delinsCAA
|
XP_011538283.1:p.Trp274Gln
|
|
XM_011539982.1:c.724_726delinsCAA
|
XP_011538284.1:p.Trp242Gln
|
|
XR_945791.1:n.1390_1392delinsCAA
|
|
|
NM_000314.7:c.820_822delinsCAA
|
NP_000305.3:p.Trp274Gln
|
|
NM_001304717.5:c.1339_1341delinsCAA
|
NP_001291646.4:p.Trp447Gln
|
|
NM_001304718.2:c.229_231delinsCAA
|
NP_001291647.1:p.Trp77Gln
|
|
NM_000314.8:c.820_822delinsCAA
MANE Select
|
NP_000305.3:p.Trp274Gln
|
|