ENST00000700029.2:c.1084_1086delinsATG
|
ENSP00000514759.2:p.Asp362Met
|
|
ENST00000710265.1:c.991_993delinsATG
|
ENSP00000518161.1:p.Asp331Met
|
|
ENST00000472832.3:c.991_993delinsATG
|
ENSP00000483066.2:p.Asp331Met
|
|
ENST00000688158.2:n.1726_1728delinsATG
|
|
|
ENST00000688922.2:c.*821_*823delinsATG
|
ENSP00000508742.2:n.*821_*823delinsATG
|
|
ENST00000700021.1:c.946_948delinsATG
|
ENSP00000514757.1:p.Asp316Met
|
|
ENST00000700022.1:c.*330_*332delinsATG
|
ENSP00000514758.1:n.*330_*332delinsATG
|
|
ENST00000700023.1:n.2149_2151delinsATG
|
|
|
ENST00000700024.1:n.2383_2385delinsATG
|
|
|
ENST00000700025.1:n.1760_1762delinsATG
|
|
|
ENST00000700026.1:n.628_630delinsATG
|
|
|
ENST00000706954.1:c.991_993delinsATG
|
ENSP00000516674.1:p.Asp331Met
|
|
ENST00000706955.1:c.*1026_*1028delinsATG
|
ENSP00000516675.1:n.*1026_*1028delinsATG
|
|
ENST00000686459.1:c.*577_*579delinsATG
|
ENSP00000508909.1:n.*577_*579delinsATG
|
|
ENST00000688158.1:c.*1102_*1104delinsATG
|
ENSP00000509254.1:n.*1102_*1104delinsATG
|
|
ENST00000688308.1:c.991_993delinsATG
|
ENSP00000508752.1:p.Asp331Met
|
|
ENST00000688922.1:c.912_914delinsATG
|
|
|
ENST00000693560.1:c.1510_1512delinsATG
|
ENSP00000509861.1:p.Asp504Met
|
|
ENST00000371953.8:c.991_993delinsATG
MANE Select
|
ENSP00000361021.3:p.Asp331Met
|
|
ENST00000371953.7:c.991_993delinsATG
|
ENSP00000361021.3:p.Asp331Met
|
|
ENST00000472832.2:c.418_420delinsATG
|
ENSP00000483066.1:p.Asp140Met
|
|
NM_000314.5:c.991_993delinsATG
|
NP_000305.3:p.Asp331Met
|
|
NM_000314.6:c.991_993delinsATG
|
NP_000305.3:p.Asp331Met
|
|
NM_001304717.2:c.1510_1512delinsATG
|
NP_001291646.2:p.Asp504Met
|
|
NM_001304718.1:c.400_402delinsATG
|
NP_001291647.1:p.Asp134Met
|
|
XM_006717926.2:c.946_948delinsATG
|
XP_006717989.1:p.Asp316Met
|
|
XM_011539981.1:c.991_993delinsATG
|
XP_011538283.1:p.Asp331Met
|
|
XM_011539982.1:c.895_897delinsATG
|
XP_011538284.1:p.Asp299Met
|
|
XR_945791.1:n.1561_1563delinsATG
|
|
|
NM_000314.7:c.991_993delinsATG
|
NP_000305.3:p.Asp331Met
|
|
NM_001304717.5:c.1510_1512delinsATG
|
NP_001291646.4:p.Asp504Met
|
|
NM_001304718.2:c.400_402delinsATG
|
NP_001291647.1:p.Asp134Met
|
|
NM_000314.8:c.991_993delinsATG
MANE Select
|
NP_000305.3:p.Asp331Met
|
|