ENST00000700029.2:c.526_528delinsCAA
|
ENSP00000514759.2:p.Tyr176Gln
|
|
ENST00000710265.1:c.526_528delinsCAA
|
ENSP00000518161.1:p.Tyr176Gln
|
|
ENST00000472832.3:c.526_528delinsCAA
|
ENSP00000483066.2:p.Tyr176Gln
|
|
ENST00000688158.2:n.1261_1263delinsCAA
|
|
|
ENST00000688922.2:c.*356_*358delinsCAA
|
ENSP00000508742.2:n.*356_*358delinsCAA
|
|
ENST00000700021.1:c.481_483delinsCAA
|
ENSP00000514757.1:p.Tyr161Gln
|
|
ENST00000700022.1:c.493-5702_493-5700delinsCAA
|
ENSP00000514758.1:n.493-5702_493-5700delinsCAA
|
|
ENST00000700023.1:n.1684_1686delinsCAA
|
|
|
ENST00000700024.1:n.1918_1920delinsCAA
|
|
|
ENST00000700025.1:n.1295_1297delinsCAA
|
|
|
ENST00000700029.1:c.360_362delinsCAA
|
|
|
ENST00000706954.1:c.526_528delinsCAA
|
ENSP00000516674.1:p.Tyr176Gln
|
|
ENST00000706955.1:c.*561_*563delinsCAA
|
ENSP00000516675.1:n.*561_*563delinsCAA
|
|
ENST00000686459.1:c.*112_*114delinsCAA
|
ENSP00000508909.1:n.*112_*114delinsCAA
|
|
ENST00000688158.1:c.*637_*639delinsCAA
|
ENSP00000509254.1:n.*637_*639delinsCAA
|
|
ENST00000688308.1:c.526_528delinsCAA
|
ENSP00000508752.1:p.Tyr176Gln
|
|
ENST00000688922.1:c.447_449delinsCAA
|
|
|
ENST00000693560.1:c.1045_1047delinsCAA
|
ENSP00000509861.1:p.Tyr349Gln
|
|
ENST00000371953.8:c.526_528delinsCAA
MANE Select
|
ENSP00000361021.3:p.Tyr176Gln
|
|
ENST00000371953.7:c.526_528delinsCAA
|
ENSP00000361021.3:p.Tyr176Gln
|
|
NM_000314.5:c.526_528delinsCAA
|
NP_000305.3:p.Tyr176Gln
|
|
NM_000314.6:c.526_528delinsCAA
|
NP_000305.3:p.Tyr176Gln
|
|
NM_001304717.2:c.1045_1047delinsCAA
|
NP_001291646.2:p.Tyr349Gln
|
|
NM_001304718.1:c.-66_-64delinsCAA
|
NP_001291647.1:n.-66_-64delinsCAA
|
|
XM_006717926.2:c.481_483delinsCAA
|
XP_006717989.1:p.Tyr161Gln
|
|
XM_011539981.1:c.526_528delinsCAA
|
XP_011538283.1:p.Tyr176Gln
|
|
XM_011539982.1:c.430_432delinsCAA
|
XP_011538284.1:p.Tyr144Gln
|
|
XR_945789.1:n.1397_1399delinsCAA
|
|
|
XR_945790.1:n.1514_1516delinsCAA
|
|
|
XR_945791.1:n.1205-5702_1205-5700delinsCAA
|
|
|
NM_000314.7:c.526_528delinsCAA
|
NP_000305.3:p.Tyr176Gln
|
|
NM_001304717.5:c.1045_1047delinsCAA
|
NP_001291646.4:p.Tyr349Gln
|
|
NM_001304718.2:c.-66_-64delinsCAA
|
NP_001291647.1:n.-66_-64delinsCAA
|
|
NM_000314.8:c.526_528delinsCAA
MANE Select
|
NP_000305.3:p.Tyr176Gln
|
|