|
ENST00000265593.9:c.1183G=
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Glu395=
|
|
|
ENST00000475279.2:c.565G=
(CLCN2)
|
|
|
|
ENST00000636180.1:c.*159G=
(CLCN2)
|
ENSP00000490374.1:n.*159G=
|
|
|
ENST00000636241.1:c.1074G=
(CLCN2)
|
|
|
|
ENST00000636492.1:c.1066G=
(CLCN2)
|
ENSP00000490313.1:p.Glu356=
|
|
|
ENST00000636658.1:c.444G=
(CLCN2)
|
|
|
|
ENST00000636661.1:c.*1373G=
(CLCN2)
|
ENSP00000490764.1:n.*1373G=
|
|
|
ENST00000637392.1:n.2459G=
(CLCN2)
|
|
|
|
ENST00000637538.1:c.489G=
(CLCN2)
|
|
|
|
ENST00000637909.1:c.989G=
(CLCN2)
|
|
|
|
ENST00000638134.1:c.991G=
(CLCN2)
|
|
|
|
ENST00000265593.8:c.1183G=
(CLCN2)
|
ENSP00000265593.4:p.Glu395=
|
|
|
ENST00000344937.11:c.1183G=
(CLCN2)
|
ENSP00000345056.7:p.Glu395=
|
|
|
ENST00000430397.5:c.126G=
(CLCN2)
|
|
|
|
ENST00000434054.6:c.1051G=
(CLCN2)
|
ENSP00000400425.2:p.Glu351=
|
|
|
ENST00000444495.1:c.2106+210810C=
(EIF2B5)
|
ENSP00000409142.1:n.2106+210810C=
|
|
|
ENST00000457512.1:c.1183G=
(CLCN2)
|
ENSP00000391928.1:p.Glu395=
|
|
|
ENST00000475279.1:n.201G=
(CLCN2)
|
|
|
|
ENST00000485667.1:n.1190G=
(CLCN2)
|
|
|
|
NM_001171087.2:c.1183G=
(CLCN2)
|
NP_001164558.1:p.Glu395=
|
|
|
NM_001171088.2:c.1051G=
(CLCN2)
|
NP_001164559.1:p.Glu351=
|
|
|
NM_001171089.2:c.1183G=
(CLCN2)
|
NP_001164560.1:p.Glu395=
|
|
|
NM_004366.5:c.1183G=
(CLCN2)
|
NP_004357.3:p.Glu395=
|
|
|
XM_006713489.1:c.1183G=
(CLCN2)
|
XP_006713552.1:p.Glu395=
|
|
|
XM_006713490.1:c.25G=
(CLCN2)
|
XP_006713553.1:p.Glu9=
|
|
|
XM_011512401.1:c.1183G=
(CLCN2)
|
XP_011510703.1:p.Glu395=
|
|
|
XM_011512402.1:c.1183G=
(CLCN2)
|
XP_011510704.1:p.Glu395=
|
|
|
XM_006713490.2:c.25G=
(CLCN2)
|
XP_006713553.1:p.Glu9=
|
|
|
XR_001740001.1:n.1307G=
(CLCN2)
|
|
|
|
XR_001740002.1:n.1307G=
(CLCN2)
|
|
|
|
NM_004366.6:c.1183G=
(CLCN2)
MANE Select
|
NP_004357.3:p.Glu395=
|
|
|
NM_001171087.3:c.1183G=
(CLCN2)
|
NP_001164558.1:p.Glu395=
|
|
|
NM_001171088.3:c.1051G=
(CLCN2)
|
NP_001164559.1:p.Glu351=
|
|
|
NM_001171089.3:c.1183G=
(CLCN2)
|
NP_001164560.1:p.Glu395=
|
|
