|
NM_004366.6:c.898+1G>A
(CLCN2)
MANE Select
|
NP_004357.3:n.898+1G>A
|
|
ENST00000265593.9:c.898+1G>A
(CLCN2)
MANE Select
|
ENSP00000265593.4:n.898+1G>A
|
|
NM_001171087.2:c.898+1G>A
(CLCN2)
|
NP_001164558.1:n.898+1G>A
|
|
NM_001171087.3:c.898+1G>A
(CLCN2)
|
NP_001164558.1:n.898+1G>A
|
|
NM_001171088.2:c.766+1G>A
(CLCN2)
|
NP_001164559.1:n.766+1G>A
|
|
NM_001171088.3:c.766+1G>A
(CLCN2)
|
NP_001164559.1:n.766+1G>A
|
|
NM_001171089.2:c.898+1G>A
(CLCN2)
|
NP_001164560.1:n.898+1G>A
|
|
NM_001171089.3:c.898+1G>A
(CLCN2)
|
NP_001164560.1:n.898+1G>A
|
|
NM_004366.5:c.898+1G>A
(CLCN2)
|
NP_004357.3:n.898+1G>A
|
|
ENST00000265593.8:c.898+1G>A
(CLCN2)
|
ENSP00000265593.4:n.898+1G>A
|
|
ENST00000344937.11:c.898+1G>A
(CLCN2)
|
ENSP00000345056.7:n.898+1G>A
|
|
ENST00000434054.6:c.766+1G>A
(CLCN2)
|
ENSP00000400425.2:n.766+1G>A
|
|
ENST00000444495.1:c.2106+212654C>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+212654C>T
|
|
ENST00000457512.1:c.898+1G>A
(CLCN2)
|
ENSP00000391928.1:n.898+1G>A
|
|
ENST00000475279.2:c.214+1G>A
(CLCN2)
|
|
|
ENST00000485667.1:n.905+1G>A
(CLCN2)
|
|
|
ENST00000636180.1:c.741+1G>A
(CLCN2)
|
ENSP00000490374.1:n.741+1G>A
|
|
ENST00000636241.1:c.789+1G>A
(CLCN2)
|
|
|
ENST00000636492.1:c.781+1G>A
(CLCN2)
|
ENSP00000490313.1:n.781+1G>A
|
|
ENST00000636658.1:c.203+1G>A
(CLCN2)
|
|
|
ENST00000636661.1:c.741+1G>A
(CLCN2)
|
ENSP00000490764.1:n.741+1G>A
|
|
ENST00000636860.1:n.194+1G>A
(CLCN2)
|
|
|
ENST00000637392.1:n.796+1G>A
(CLCN2)
|
|
|
ENST00000637538.1:c.204+1G>A
(CLCN2)
|
|
|
ENST00000637909.1:c.606+1G>A
(CLCN2)
|
|
|
ENST00000638134.1:c.706+1G>A
(CLCN2)
|
|
|
XM_006713489.1:c.898+1G>A
(CLCN2)
|
XP_006713552.1:n.898+1G>A
|
|
XM_006713490.2:c.-327+1G>A
(CLCN2)
|
XP_006713553.1:n.-327+1G>A
|
|
XM_011512401.1:c.898+1G>A
(CLCN2)
|
XP_011510703.1:n.898+1G>A
|
|
XM_011512402.1:c.898+1G>A
(CLCN2)
|
XP_011510704.1:n.898+1G>A
|
|
XR_001740001.1:n.1022+1G>A
(CLCN2)
|
|
|
XR_001740002.1:n.1022+1G>A
(CLCN2)
|
|
