ENST00000265593.9:c.1192G>A
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Val398Ile
|
|
ENST00000475279.2:c.574G>A
(CLCN2)
|
|
|
ENST00000636180.1:c.*168G>A
(CLCN2)
|
ENSP00000490374.1:n.*168G>A
|
|
ENST00000636241.1:c.1083G>A
(CLCN2)
|
|
|
ENST00000636492.1:c.1075G>A
(CLCN2)
|
ENSP00000490313.1:p.Val359Ile
|
|
ENST00000636658.1:c.453G>A
(CLCN2)
|
|
|
ENST00000636661.1:c.*1382G>A
(CLCN2)
|
ENSP00000490764.1:n.*1382G>A
|
|
ENST00000637392.1:n.2468G>A
(CLCN2)
|
|
|
ENST00000637538.1:c.498G>A
(CLCN2)
|
|
|
ENST00000637909.1:c.998G>A
(CLCN2)
|
|
|
ENST00000638134.1:c.1000G>A
(CLCN2)
|
|
|
ENST00000265593.8:c.1192G>A
(CLCN2)
|
ENSP00000265593.4:p.Val398Ile
|
|
ENST00000344937.11:c.1192G>A
(CLCN2)
|
ENSP00000345056.7:p.Val398Ile
|
|
ENST00000430397.5:c.135G>A
(CLCN2)
|
|
|
ENST00000434054.6:c.1060G>A
(CLCN2)
|
ENSP00000400425.2:p.Val354Ile
|
|
ENST00000444495.1:c.2106+210801C>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+210801C>T
|
|
ENST00000457512.1:c.1192G>A
(CLCN2)
|
ENSP00000391928.1:p.Val398Ile
|
|
ENST00000475279.1:n.210G>A
(CLCN2)
|
|
|
ENST00000485667.1:n.1199G>A
(CLCN2)
|
|
|
NM_001171087.2:c.1192G>A
(CLCN2)
|
NP_001164558.1:p.Val398Ile
|
|
NM_001171088.2:c.1060G>A
(CLCN2)
|
NP_001164559.1:p.Val354Ile
|
|
NM_001171089.2:c.1192G>A
(CLCN2)
|
NP_001164560.1:p.Val398Ile
|
|
NM_004366.5:c.1192G>A
(CLCN2)
|
NP_004357.3:p.Val398Ile
|
|
XM_006713489.1:c.1192G>A
(CLCN2)
|
XP_006713552.1:p.Val398Ile
|
|
XM_006713490.1:c.34G>A
(CLCN2)
|
XP_006713553.1:p.Val12Ile
|
|
XM_011512401.1:c.1192G>A
(CLCN2)
|
XP_011510703.1:p.Val398Ile
|
|
XM_011512402.1:c.1192G>A
(CLCN2)
|
XP_011510704.1:p.Val398Ile
|
|
XM_006713490.2:c.34G>A
(CLCN2)
|
XP_006713553.1:p.Val12Ile
|
|
XR_001740001.1:n.1316G>A
(CLCN2)
|
|
|
XR_001740002.1:n.1316G>A
(CLCN2)
|
|
|
NM_004366.6:c.1192G>A
(CLCN2)
MANE Select
|
NP_004357.3:p.Val398Ile
|
|
NM_001171087.3:c.1192G>A
(CLCN2)
|
NP_001164558.1:p.Val398Ile
|
|
NM_001171088.3:c.1060G>A
(CLCN2)
|
NP_001164559.1:p.Val354Ile
|
|
NM_001171089.3:c.1192G>A
(CLCN2)
|
NP_001164560.1:p.Val398Ile
|
|