|
ENST00000700029.2:c.792_795delinsGCTA
|
ENSP00000514759.2:p.Met264=
|
|
|
ENST00000710265.1:c.792_795delinsGCTA
|
ENSP00000518161.1:p.Met264=
|
|
|
ENST00000472832.3:c.792_795delinsGCTA
|
ENSP00000483066.2:p.Met264=
|
|
|
ENST00000688158.2:n.1527_1530delinsGCTA
|
|
|
|
ENST00000688922.2:c.*622_*625delinsGCTA
|
ENSP00000508742.2:n.*622_*625delinsGCTA
|
|
|
ENST00000700021.1:c.747_750delinsGCTA
|
ENSP00000514757.1:p.Met249=
|
|
|
ENST00000700022.1:c.*131_*134delinsGCTA
|
ENSP00000514758.1:n.*131_*134delinsGCTA
|
|
|
ENST00000700023.1:n.1950_1953delinsGCTA
|
|
|
|
ENST00000700024.1:n.2184_2187delinsGCTA
|
|
|
|
ENST00000700025.1:n.1561_1564delinsGCTA
|
|
|
|
ENST00000700026.1:n.429_432delinsGCTA
|
|
|
|
ENST00000700029.1:c.626_629delinsGCTA
|
|
|
|
ENST00000706954.1:c.792_795delinsGCTA
|
ENSP00000516674.1:p.Met264=
|
|
|
ENST00000706955.1:c.*827_*830delinsGCTA
|
ENSP00000516675.1:n.*827_*830delinsGCTA
|
|
|
ENST00000686459.1:c.*378_*381delinsGCTA
|
ENSP00000508909.1:n.*378_*381delinsGCTA
|
|
|
ENST00000688158.1:c.*903_*906delinsGCTA
|
ENSP00000509254.1:n.*903_*906delinsGCTA
|
|
|
ENST00000688308.1:c.792_795delinsGCTA
|
ENSP00000508752.1:p.Met264=
|
|
|
ENST00000688922.1:c.713_716delinsGCTA
|
|
|
|
ENST00000693560.1:c.1311_1314delinsGCTA
|
ENSP00000509861.1:p.Met437=
|
|
|
ENST00000371953.8:c.792_795delinsGCTA
MANE Select
|
ENSP00000361021.3:p.Met264=
|
|
|
ENST00000371953.7:c.792_795delinsGCTA
|
ENSP00000361021.3:p.Met264=
|
|
|
ENST00000472832.2:c.219_222delinsGCTA
|
ENSP00000483066.1:p.Met73=
|
|
|
NM_000314.5:c.792_795delinsGCTA
|
NP_000305.3:p.Met264=
|
|
|
NM_000314.6:c.792_795delinsGCTA
|
NP_000305.3:p.Met264=
|
|
|
NM_001304717.2:c.1311_1314delinsGCTA
|
NP_001291646.2:p.Met437=
|
|
|
NM_001304718.1:c.201_204delinsGCTA
|
NP_001291647.1:p.Met67=
|
|
|
XM_006717926.2:c.747_750delinsGCTA
|
XP_006717989.1:p.Met249=
|
|
|
XM_011539981.1:c.792_795delinsGCTA
|
XP_011538283.1:p.Met264=
|
|
|
XM_011539982.1:c.696_699delinsGCTA
|
XP_011538284.1:p.Met232=
|
|
|
XR_945791.1:n.1362_1365delinsGCTA
|
|
|
|
NM_000314.7:c.792_795delinsGCTA
|
NP_000305.3:p.Met264=
|
|
|
NM_001304717.5:c.1311_1314delinsGCTA
|
NP_001291646.4:p.Met437=
|
|
|
NM_001304718.2:c.201_204delinsGCTA
|
NP_001291647.1:p.Met67=
|
|
|
NM_000314.8:c.792_795delinsGCTA
MANE Select
|
NP_000305.3:p.Met264=
|
|
