ENST00000334571.7:c.497T>G
(COQ6)
MANE Select
|
ENSP00000333946.2:p.Leu166Arg
|
|
ENST00000238709.8:c.494T>G
(COQ6)
|
ENSP00000238709.5:p.Leu165Arg
|
|
ENST00000334571.6:c.497T>G
(COQ6)
|
ENSP00000333946.2:p.Leu166Arg
|
|
ENST00000394026.8:c.422T>G
(COQ6)
|
ENSP00000377594.4:p.Leu141Arg
|
|
ENST00000553462.6:n.345T>G
(COQ6)
|
|
|
ENST00000554153.5:c.*102T>G
(COQ6)
|
ENSP00000451685.1:n.*102T>G
|
|
ENST00000554320.1:c.272T>G
(COQ6)
|
ENSP00000451123.1:p.Leu91Arg
|
|
ENST00000554341.6:c.*102T>G
(COQ6)
|
ENSP00000450736.2:n.*102T>G
|
|
ENST00000554920.5:c.481+2234T>G
(COQ6)
|
ENSP00000451562.1:n.481+2234T>G
|
|
ENST00000555511.5:n.615T>G
(COQ6)
|
|
|
ENST00000556300.6:n.531T>G
(COQ6)
|
|
|
ENST00000557205.6:n.461T>G
(COQ6)
|
|
|
ENST00000557325.5:c.*1368A>C
(ENTPD5)
|
ENSP00000451810.1:n.*1368A>C
|
|
ENST00000557584.5:c.*102T>G
(COQ6)
|
ENSP00000450511.1:n.*102T>G
|
|
ENST00000629426.2:c.272T>G
(COQ6)
|
ENSP00000486650.1:p.Leu91Arg
|
|
NM_182476.2:c.497T>G
(COQ6)
|
NP_872282.1:p.Leu166Arg
|
|
NM_182480.2:c.422T>G
(COQ6)
|
NP_872286.2:p.Leu141Arg
|
|
XM_005267716.1:c.332T>G
(COQ6)
|
XP_005267773.1:p.Leu111Arg
|
|
XM_006720156.1:c.170T>G
(COQ6)
|
XP_006720219.1:p.Leu57Arg
|
|
XM_011536807.1:c.497T>G
(COQ6)
|
XP_011535109.1:p.Leu166Arg
|
|
XM_011536808.1:c.272T>G
(COQ6)
|
XP_011535110.1:p.Leu91Arg
|
|
XM_011536809.1:c.272T>G
(COQ6)
|
XP_011535111.1:p.Leu91Arg
|
|
XM_011536810.1:c.497T>G
(COQ6)
|
XP_011535112.1:p.Leu166Arg
|
|
XM_011536811.1:c.73-809T>G
(COQ6)
|
XP_011535113.1:n.73-809T>G
|
|
XR_943465.1:n.550T>G
(COQ6)
|
|
|
XR_943466.1:n.550T>G
(COQ6)
|
|
|
NM_001330189.1:c.*1368A>C
(ENTPD5)
|
NP_001317118.1:n.*1368A>C
|
|
XM_011536807.2:c.497T>G
(COQ6)
|
XP_011535109.1:p.Leu166Arg
|
|
XM_011536808.2:c.272T>G
(COQ6)
|
XP_011535110.1:p.Leu91Arg
|
|
XM_011536809.3:c.272T>G
(COQ6)
|
XP_011535111.1:p.Leu91Arg
|
|
XM_011536810.3:c.497T>G
(COQ6)
|
XP_011535112.1:p.Leu166Arg
|
|
XM_017021351.2:c.73-809T>G
(COQ6)
|
XP_016876840.1:n.73-809T>G
|
|
XM_017021352.2:c.-803T>G
(COQ6)
|
XP_016876841.1:n.-803T>G
|
|
XM_024449619.1:c.-252T>G
(COQ6)
|
XP_024305387.1:n.-252T>G
|
|
XR_001750342.1:n.461T>G
(COQ6)
|
|
|
XR_943465.3:n.527T>G
(COQ6)
|
|
|
XR_943466.3:n.527T>G
(COQ6)
|
|
|
NM_001330189.2:c.*1368A>C
(ENTPD5)
|
NP_001317118.1:n.*1368A>C
|
|
NM_182476.3:c.497T>G
(COQ6)
MANE Select
|
NP_872282.1:p.Leu166Arg
|
|
NM_001382258.1:c.1201-2575A>C
(ENTPD5)
|
NP_001369187.1:n.1201-2575A>C
|
|
NM_001382259.1:c.*1368A>C
(ENTPD5)
|
NP_001369188.1:n.*1368A>C
|
|
NM_001382260.1:c.*1368A>C
(ENTPD5)
|
NP_001369189.1:n.*1368A>C
|
|
NM_001382262.1:c.1201-2334A>C
(ENTPD5)
|
NP_001369191.1:n.1201-2334A>C
|
|
NM_182480.3:c.422T>G
(COQ6)
|
NP_872286.2:p.Leu141Arg
|
|