|
ENST00000265593.9:c.1134C>G
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Thr378=
|
|
|
ENST00000475279.2:c.516C>G
(CLCN2)
|
|
|
|
ENST00000636180.1:c.*110C>G
(CLCN2)
|
ENSP00000490374.1:n.*110C>G
|
|
|
ENST00000636241.1:c.1025C>G
(CLCN2)
|
|
|
|
ENST00000636492.1:c.1017C>G
(CLCN2)
|
ENSP00000490313.1:p.Thr339=
|
|
|
ENST00000636658.1:c.395C>G
(CLCN2)
|
|
|
|
ENST00000636661.1:c.*1324C>G
(CLCN2)
|
ENSP00000490764.1:n.*1324C>G
|
|
|
ENST00000637392.1:n.2246C>G
(CLCN2)
|
|
|
|
ENST00000637538.1:c.440C>G
(CLCN2)
|
|
|
|
ENST00000637909.1:c.940C>G
(CLCN2)
|
|
|
|
ENST00000638134.1:c.942C>G
(CLCN2)
|
|
|
|
ENST00000265593.8:c.1134C>G
(CLCN2)
|
ENSP00000265593.4:p.Thr378=
|
|
|
ENST00000344937.11:c.1134C>G
(CLCN2)
|
ENSP00000345056.7:p.Thr378=
|
|
|
ENST00000430397.5:c.77C>G
(CLCN2)
|
|
|
|
ENST00000434054.6:c.1002C>G
(CLCN2)
|
ENSP00000400425.2:p.Thr334=
|
|
|
ENST00000444495.1:c.2106+211023G>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+211023G>C
|
|
|
ENST00000457512.1:c.1134C>G
(CLCN2)
|
ENSP00000391928.1:p.Thr378=
|
|
|
ENST00000475279.1:n.152C>G
(CLCN2)
|
|
|
|
ENST00000485667.1:n.1141C>G
(CLCN2)
|
|
|
|
NM_001171087.2:c.1134C>G
(CLCN2)
|
NP_001164558.1:p.Thr378=
|
|
|
NM_001171088.2:c.1002C>G
(CLCN2)
|
NP_001164559.1:p.Thr334=
|
|
|
NM_001171089.2:c.1134C>G
(CLCN2)
|
NP_001164560.1:p.Thr378=
|
|
|
NM_004366.5:c.1134C>G
(CLCN2)
|
NP_004357.3:p.Thr378=
|
|
|
XM_006713489.1:c.1134C>G
(CLCN2)
|
XP_006713552.1:p.Thr378=
|
|
|
XM_006713490.1:c.-25C>G
(CLCN2)
|
XP_006713553.1:n.-25C>G
|
|
|
XM_011512401.1:c.1134C>G
(CLCN2)
|
XP_011510703.1:p.Thr378=
|
|
|
XM_011512402.1:c.1134C>G
(CLCN2)
|
XP_011510704.1:p.Thr378=
|
|
|
XM_006713490.2:c.-25C>G
(CLCN2)
|
XP_006713553.1:n.-25C>G
|
|
|
XR_001740001.1:n.1258C>G
(CLCN2)
|
|
|
|
XR_001740002.1:n.1258C>G
(CLCN2)
|
|
|
|
NM_004366.6:c.1134C>G
(CLCN2)
MANE Select
|
NP_004357.3:p.Thr378=
|
|
|
NM_001171087.3:c.1134C>G
(CLCN2)
|
NP_001164558.1:p.Thr378=
|
|
|
NM_001171088.3:c.1002C>G
(CLCN2)
|
NP_001164559.1:p.Thr334=
|
|
|
NM_001171089.3:c.1134C>G
(CLCN2)
|
NP_001164560.1:p.Thr378=
|
|
