|
ENST00000700029.2:c.790_792delinsGAT
|
ENSP00000514759.2:p.Met264Asp
|
|
|
ENST00000710265.1:c.790_792delinsGAT
|
ENSP00000518161.1:p.Met264Asp
|
|
|
ENST00000472832.3:c.790_792delinsGAT
|
ENSP00000483066.2:p.Met264Asp
|
|
|
ENST00000688158.2:n.1525_1527delinsGAT
|
|
|
|
ENST00000688922.2:c.*620_*622delinsGAT
|
ENSP00000508742.2:n.*620_*622delinsGAT
|
|
|
ENST00000700021.1:c.745_747delinsGAT
|
ENSP00000514757.1:p.Met249Asp
|
|
|
ENST00000700022.1:c.*129_*131delinsGAT
|
ENSP00000514758.1:n.*129_*131delinsGAT
|
|
|
ENST00000700023.1:n.1948_1950delinsGAT
|
|
|
|
ENST00000700024.1:n.2182_2184delinsGAT
|
|
|
|
ENST00000700025.1:n.1559_1561delinsGAT
|
|
|
|
ENST00000700026.1:n.427_429delinsGAT
|
|
|
|
ENST00000700029.1:c.624_626delinsGAT
|
|
|
|
ENST00000706954.1:c.790_792delinsGAT
|
ENSP00000516674.1:p.Met264Asp
|
|
|
ENST00000706955.1:c.*825_*827delinsGAT
|
ENSP00000516675.1:n.*825_*827delinsGAT
|
|
|
ENST00000686459.1:c.*376_*378delinsGAT
|
ENSP00000508909.1:n.*376_*378delinsGAT
|
|
|
ENST00000688158.1:c.*901_*903delinsGAT
|
ENSP00000509254.1:n.*901_*903delinsGAT
|
|
|
ENST00000688308.1:c.790_792delinsGAT
|
ENSP00000508752.1:p.Met264Asp
|
|
|
ENST00000688922.1:c.711_713delinsGAT
|
|
|
|
ENST00000693560.1:c.1309_1311delinsGAT
|
ENSP00000509861.1:p.Met437Asp
|
|
|
ENST00000371953.8:c.790_792delinsGAT
MANE Select
|
ENSP00000361021.3:p.Met264Asp
|
|
|
ENST00000371953.7:c.790_792delinsGAT
|
ENSP00000361021.3:p.Met264Asp
|
|
|
ENST00000472832.2:c.217_219delinsGAT
|
ENSP00000483066.1:p.Met73Asp
|
|
|
NM_000314.5:c.790_792delinsGAT
|
NP_000305.3:p.Met264Asp
|
|
|
NM_000314.6:c.790_792delinsGAT
|
NP_000305.3:p.Met264Asp
|
|
|
NM_001304717.2:c.1309_1311delinsGAT
|
NP_001291646.2:p.Met437Asp
|
|
|
NM_001304718.1:c.199_201delinsGAT
|
NP_001291647.1:p.Met67Asp
|
|
|
XM_006717926.2:c.745_747delinsGAT
|
XP_006717989.1:p.Met249Asp
|
|
|
XM_011539981.1:c.790_792delinsGAT
|
XP_011538283.1:p.Met264Asp
|
|
|
XM_011539982.1:c.694_696delinsGAT
|
XP_011538284.1:p.Met232Asp
|
|
|
XR_945791.1:n.1360_1362delinsGAT
|
|
|
|
NM_000314.7:c.790_792delinsGAT
|
NP_000305.3:p.Met264Asp
|
|
|
NM_001304717.5:c.1309_1311delinsGAT
|
NP_001291646.4:p.Met437Asp
|
|
|
NM_001304718.2:c.199_201delinsGAT
|
NP_001291647.1:p.Met67Asp
|
|
|
NM_000314.8:c.790_792delinsGAT
MANE Select
|
NP_000305.3:p.Met264Asp
|
|
