ENST00000700029.2:c.744_745insC
|
ENSP00000514759.2:p.Val249ArgfsTer4
|
|
ENST00000710265.1:c.744_745insC
|
ENSP00000518161.1:p.Val249ArgfsTer4
|
|
ENST00000472832.3:c.744_745insC
|
ENSP00000483066.2:p.Val249ArgfsTer4
|
|
ENST00000688158.2:n.1479_1480insC
|
|
|
ENST00000688922.2:c.*574_*575insC
|
ENSP00000508742.2:n.*574_*575insC
|
|
ENST00000700021.1:c.699_700insC
|
ENSP00000514757.1:p.Val234ArgfsTer4
|
|
ENST00000700022.1:c.*83_*84insC
|
ENSP00000514758.1:n.*83_*84insC
|
|
ENST00000700023.1:n.1902_1903insC
|
|
|
ENST00000700024.1:n.2136_2137insC
|
|
|
ENST00000700025.1:n.1513_1514insC
|
|
|
ENST00000700026.1:n.381_382insC
|
|
|
ENST00000700029.1:c.578_579insC
|
|
|
ENST00000706954.1:c.744_745insC
|
ENSP00000516674.1:p.Val249ArgfsTer4
|
|
ENST00000706955.1:c.*779_*780insC
|
ENSP00000516675.1:n.*779_*780insC
|
|
ENST00000686459.1:c.*330_*331insC
|
ENSP00000508909.1:n.*330_*331insC
|
|
ENST00000688158.1:c.*855_*856insC
|
ENSP00000509254.1:n.*855_*856insC
|
|
ENST00000688308.1:c.744_745insC
|
ENSP00000508752.1:p.Val249ArgfsTer4
|
|
ENST00000688922.1:c.665_666insC
|
|
|
ENST00000693560.1:c.1263_1264insC
|
ENSP00000509861.1:p.Val422ArgfsTer4
|
|
ENST00000371953.8:c.744_745insC
MANE Select
|
ENSP00000361021.3:p.Val249ArgfsTer4
|
|
ENST00000371953.7:c.744_745insC
|
ENSP00000361021.3:p.Val249ArgfsTer4
|
|
ENST00000472832.2:c.171_172insC
|
ENSP00000483066.1:p.Val58ArgfsTer4
|
|
NM_000314.5:c.744_745insC
|
NP_000305.3:p.Val249ArgfsTer4
|
|
NM_000314.6:c.744_745insC
|
NP_000305.3:p.Val249ArgfsTer4
|
|
NM_001304717.2:c.1263_1264insC
|
NP_001291646.2:p.Val422ArgfsTer4
|
|
NM_001304718.1:c.153_154insC
|
NP_001291647.1:p.Val52ArgfsTer4
|
|
XM_006717926.2:c.699_700insC
|
XP_006717989.1:p.Val234ArgfsTer4
|
|
XM_011539981.1:c.744_745insC
|
XP_011538283.1:p.Val249ArgfsTer4
|
|
XM_011539982.1:c.648_649insC
|
XP_011538284.1:p.Val217ArgfsTer4
|
|
XR_945791.1:n.1314_1315insC
|
|
|
NM_000314.7:c.744_745insC
|
NP_000305.3:p.Val249ArgfsTer4
|
|
NM_001304717.5:c.1263_1264insC
|
NP_001291646.4:p.Val422ArgfsTer4
|
|
NM_001304718.2:c.153_154insC
|
NP_001291647.1:p.Val52ArgfsTer4
|
|
NM_000314.8:c.744_745insC
MANE Select
|
NP_000305.3:p.Val249ArgfsTer4
|
|