ENST00000607635.2:c.756G>A
|
ENSP00000496683.1:p.Glu252=
|
|
ENST00000642195.1:c.756G>A
MANE Select
|
ENSP00000496044.1:p.Glu252=
|
|
ENST00000643341.1:c.756G>A
|
ENSP00000496018.1:p.Glu252=
|
|
ENST00000643799.1:c.656-207G>A
|
ENSP00000494529.1:n.656-207G>A
|
|
ENST00000645141.1:c.*367G>A
|
ENSP00000496755.1:n.*367G>A
|
|
ENST00000646188.1:c.591G>A
|
ENSP00000496001.1:p.Glu197=
|
|
ENST00000646433.1:c.756G>A
|
ENSP00000494368.1:p.Glu252=
|
|
ENST00000646700.1:c.756G>A
|
ENSP00000495521.1:p.Glu252=
|
|
ENST00000304004.7:c.756G>A
|
ENSP00000307212.3:p.Glu252=
|
|
ENST00000372344.6:c.656-207G>A
|
ENSP00000361419.2:n.656-207G>A
|
|
ENST00000372389.7:c.756G>A
|
ENSP00000361465.3:p.Glu252=
|
|
ENST00000455605.2:n.1246G>A
|
|
|
ENST00000481352.6:n.1128G>A
|
|
|
NM_203290.2:c.756G>A
|
NP_976035.1:p.Glu252=
|
|
XM_005249491.1:c.756G>A
|
XP_005249548.1:p.Glu252=
|
|
XM_011515000.1:c.756G>A
|
XP_011513302.1:p.Glu252=
|
|
NM_001318876.1:c.756G>A
|
NP_001305805.1:p.Glu252=
|
|
NM_001363658.1:c.756G>A
|
NP_001350587.1:p.Glu252=
|
|
NM_203290.3:c.756G>A
|
NP_976035.1:p.Glu252=
|
|
NM_203290.4:c.756G>A
MANE Select
|
NP_976035.1:p.Glu252=
|
|
NM_001363658.2:c.756G>A
|
NP_001350587.1:p.Glu252=
|
|
NM_001318876.2:c.756G>A
|
NP_001305805.1:p.Glu252=
|
|