ENST00000700029.2:c.525_528delinsGTAT
|
ENSP00000514759.2:p.Val175=
|
|
ENST00000710265.1:c.525_528delinsGTAT
|
ENSP00000518161.1:p.Val175=
|
|
ENST00000472832.3:c.525_528delinsGTAT
|
ENSP00000483066.2:p.Val175=
|
|
ENST00000688158.2:n.1260_1263delinsGTAT
|
|
|
ENST00000688922.2:c.*355_*358delinsGTAT
|
ENSP00000508742.2:n.*355_*358delinsGTAT
|
|
ENST00000700021.1:c.480_483delinsGTAT
|
ENSP00000514757.1:p.Val160=
|
|
ENST00000700022.1:c.493-5703_493-5700delinsGTAT
|
ENSP00000514758.1:n.493-5703_493-5700delinsGTAT
|
|
ENST00000700023.1:n.1683_1686delinsGTAT
|
|
|
ENST00000700024.1:n.1917_1920delinsGTAT
|
|
|
ENST00000700025.1:n.1294_1297delinsGTAT
|
|
|
ENST00000700029.1:c.359_362delinsGTAT
|
|
|
ENST00000706954.1:c.525_528delinsGTAT
|
ENSP00000516674.1:p.Val175=
|
|
ENST00000706955.1:c.*560_*563delinsGTAT
|
ENSP00000516675.1:n.*560_*563delinsGTAT
|
|
ENST00000686459.1:c.*111_*114delinsGTAT
|
ENSP00000508909.1:n.*111_*114delinsGTAT
|
|
ENST00000688158.1:c.*636_*639delinsGTAT
|
ENSP00000509254.1:n.*636_*639delinsGTAT
|
|
ENST00000688308.1:c.525_528delinsGTAT
|
ENSP00000508752.1:p.Val175=
|
|
ENST00000688922.1:c.446_449delinsGTAT
|
|
|
ENST00000693560.1:c.1044_1047delinsGTAT
|
ENSP00000509861.1:p.Val348=
|
|
ENST00000371953.8:c.525_528delinsGTAT
MANE Select
|
ENSP00000361021.3:p.Val175=
|
|
ENST00000371953.7:c.525_528delinsGTAT
|
ENSP00000361021.3:p.Val175=
|
|
NM_000314.5:c.525_528delinsGTAT
|
NP_000305.3:p.Val175=
|
|
NM_000314.6:c.525_528delinsGTAT
|
NP_000305.3:p.Val175=
|
|
NM_001304717.2:c.1044_1047delinsGTAT
|
NP_001291646.2:p.Val348=
|
|
NM_001304718.1:c.-67_-64delinsGTAT
|
NP_001291647.1:n.-67_-64delinsGTAT
|
|
XM_006717926.2:c.480_483delinsGTAT
|
XP_006717989.1:p.Val160=
|
|
XM_011539981.1:c.525_528delinsGTAT
|
XP_011538283.1:p.Val175=
|
|
XM_011539982.1:c.429_432delinsGTAT
|
XP_011538284.1:p.Val143=
|
|
XR_945789.1:n.1396_1399delinsGTAT
|
|
|
XR_945790.1:n.1513_1516delinsGTAT
|
|
|
XR_945791.1:n.1205-5703_1205-5700delinsGTAT
|
|
|
NM_000314.7:c.525_528delinsGTAT
|
NP_000305.3:p.Val175=
|
|
NM_001304717.5:c.1044_1047delinsGTAT
|
NP_001291646.4:p.Val348=
|
|
NM_001304718.2:c.-67_-64delinsGTAT
|
NP_001291647.1:n.-67_-64delinsGTAT
|
|
NM_000314.8:c.525_528delinsGTAT
MANE Select
|
NP_000305.3:p.Val175=
|
|