ENST00000265593.9:c.2328G>C
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Glu776Asp
|
|
ENST00000636180.1:c.*1226G>C
(CLCN2)
|
ENSP00000490374.1:n.*1226G>C
|
|
ENST00000636661.1:c.*2638G>C
(CLCN2)
|
ENSP00000490764.1:n.*2638G>C
|
|
ENST00000637392.1:n.3870G>C
(CLCN2)
|
|
|
ENST00000637909.1:c.2134G>C
(CLCN2)
|
|
|
ENST00000265593.8:c.2328G>C
(CLCN2)
|
ENSP00000265593.4:p.Glu776Asp
|
|
ENST00000344937.11:c.2277G>C
(CLCN2)
|
ENSP00000345056.7:p.Glu759Asp
|
|
ENST00000430397.5:c.1177+193G>C
(CLCN2)
|
|
|
ENST00000434054.6:c.2196G>C
(CLCN2)
|
ENSP00000400425.2:p.Glu732Asp
|
|
ENST00000444495.1:c.2106+207393C>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+207393C>G
|
|
ENST00000457512.1:c.2328G>C
(CLCN2)
|
ENSP00000391928.1:p.Glu776Asp
|
|
NM_001171087.2:c.2277G>C
(CLCN2)
|
NP_001164558.1:p.Glu759Asp
|
|
NM_001171088.2:c.2196G>C
(CLCN2)
|
NP_001164559.1:p.Glu732Asp
|
|
NM_001171089.2:c.2328G>C
(CLCN2)
|
NP_001164560.1:p.Glu776Asp
|
|
NM_004366.5:c.2328G>C
(CLCN2)
|
NP_004357.3:p.Glu776Asp
|
|
XM_006713489.1:c.2310+193G>C
(CLCN2)
|
XP_006713552.1:n.2310+193G>C
|
|
XM_006713490.1:c.1170G>C
(CLCN2)
|
XP_006713553.1:p.Glu390Asp
|
|
XM_011512401.1:c.2328G>C
(CLCN2)
|
XP_011510703.1:p.Glu776Asp
|
|
XM_006713490.2:c.1170G>C
(CLCN2)
|
XP_006713553.1:p.Glu390Asp
|
|
XR_001740001.1:n.2508G>C
(CLCN2)
|
|
|
XR_001740002.1:n.2490+193G>C
(CLCN2)
|
|
|
NM_004366.6:c.2328G>C
(CLCN2)
MANE Select
|
NP_004357.3:p.Glu776Asp
|
|
NM_001171087.3:c.2277G>C
(CLCN2)
|
NP_001164558.1:p.Glu759Asp
|
|
NM_001171088.3:c.2196G>C
(CLCN2)
|
NP_001164559.1:p.Glu732Asp
|
|
NM_001171089.3:c.2328G>C
(CLCN2)
|
NP_001164560.1:p.Glu776Asp
|
|