ENST00000338468.8:c.1234G>A
|
ENSP00000343589.4:n.1234G>A
|
|
ENST00000366894.6:c.1115G>A
|
ENSP00000355860.2:n.1115G>A
|
|
ENST00000366898.6:c.1356G>A
MANE Select
|
ENSP00000355865.1:p.Glu452=
|
|
ENST00000673871.1:c.1437G>A
|
|
|
ENST00000674006.1:n.741G>A
|
|
|
ENST00000674436.1:n.992G>A
|
|
|
ENST00000338468.7:c.783G>A
|
ENSP00000343589.3:p.Glu261=
|
|
ENST00000366894.5:c.783G>A
|
ENSP00000355860.1:p.Glu261=
|
|
ENST00000366896.5:c.909G>A
|
ENSP00000355862.1:p.Glu303=
|
|
ENST00000366897.5:c.1272G>A
|
ENSP00000355863.1:p.Glu424=
|
|
ENST00000366898.5:c.1356G>A
|
ENSP00000355865.1:p.Glu452=
|
|
ENST00000479615.5:c.*132G>A
|
ENSP00000434414.1:n.*132G>A
|
|
ENST00000610470.4:c.489G>A
|
ENSP00000483773.1:p.Glu163=
|
|
NM_004562.2:c.1356G>A
|
NP_004553.2:p.Glu452=
|
|
NM_013987.2:c.1272G>A
|
NP_054642.2:p.Glu424=
|
|
NM_013988.2:c.909G>A
|
NP_054643.2:p.Glu303=
|
|
XM_011535863.1:c.1353G>A
|
XP_011534165.1:p.Glu451=
|
|
XM_017010908.1:c.1470G>A
|
XP_016866397.1:p.Glu490=
|
|
XM_017010909.2:c.1116G>A
|
XP_016866398.1:p.Glu372=
|
|
XM_024446449.1:c.1119G>A
|
XP_024302217.1:p.Glu373=
|
|
XR_001743443.2:n.1548G>A
|
|
|
NM_004562.3:c.1356G>A
MANE Select
|
NP_004553.2:p.Glu452=
|
|
NM_013987.3:c.1272G>A
|
NP_054642.2:p.Glu424=
|
|
NM_013988.3:c.909G>A
|
NP_054643.2:p.Glu303=
|
|