ENST00000265593.9:c.1210C>T
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Arg404Trp
|
|
ENST00000475279.2:c.592C>T
(CLCN2)
|
|
|
ENST00000636180.1:c.*186C>T
(CLCN2)
|
ENSP00000490374.1:n.*186C>T
|
|
ENST00000636241.1:c.1101C>T
(CLCN2)
|
|
|
ENST00000636492.1:c.1093C>T
(CLCN2)
|
ENSP00000490313.1:p.Arg365Trp
|
|
ENST00000636658.1:c.471C>T
(CLCN2)
|
|
|
ENST00000636661.1:c.*1400C>T
(CLCN2)
|
ENSP00000490764.1:n.*1400C>T
|
|
ENST00000637392.1:n.2486C>T
(CLCN2)
|
|
|
ENST00000637538.1:c.516C>T
(CLCN2)
|
|
|
ENST00000637909.1:c.1016C>T
(CLCN2)
|
|
|
ENST00000638134.1:c.1018C>T
(CLCN2)
|
|
|
ENST00000265593.8:c.1210C>T
(CLCN2)
|
ENSP00000265593.4:p.Arg404Trp
|
|
ENST00000344937.11:c.1210C>T
(CLCN2)
|
ENSP00000345056.7:p.Arg404Trp
|
|
ENST00000430397.5:c.153C>T
(CLCN2)
|
|
|
ENST00000434054.6:c.1078C>T
(CLCN2)
|
ENSP00000400425.2:p.Arg360Trp
|
|
ENST00000444495.1:c.2106+210783G>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+210783G>A
|
|
ENST00000457512.1:c.1210C>T
(CLCN2)
|
ENSP00000391928.1:p.Arg404Trp
|
|
ENST00000475279.1:n.228C>T
(CLCN2)
|
|
|
ENST00000485667.1:n.1217C>T
(CLCN2)
|
|
|
NM_001171087.2:c.1210C>T
(CLCN2)
|
NP_001164558.1:p.Arg404Trp
|
|
NM_001171088.2:c.1078C>T
(CLCN2)
|
NP_001164559.1:p.Arg360Trp
|
|
NM_001171089.2:c.1210C>T
(CLCN2)
|
NP_001164560.1:p.Arg404Trp
|
|
NM_004366.5:c.1210C>T
(CLCN2)
|
NP_004357.3:p.Arg404Trp
|
|
XM_006713489.1:c.1210C>T
(CLCN2)
|
XP_006713552.1:p.Arg404Trp
|
|
XM_006713490.1:c.52C>T
(CLCN2)
|
XP_006713553.1:p.Arg18Trp
|
|
XM_011512401.1:c.1210C>T
(CLCN2)
|
XP_011510703.1:p.Arg404Trp
|
|
XM_011512402.1:c.1210C>T
(CLCN2)
|
XP_011510704.1:p.Arg404Trp
|
|
XM_006713490.2:c.52C>T
(CLCN2)
|
XP_006713553.1:p.Arg18Trp
|
|
XR_001740001.1:n.1334C>T
(CLCN2)
|
|
|
XR_001740002.1:n.1334C>T
(CLCN2)
|
|
|
NM_004366.6:c.1210C>T
(CLCN2)
MANE Select
|
NP_004357.3:p.Arg404Trp
|
|
NM_001171087.3:c.1210C>T
(CLCN2)
|
NP_001164558.1:p.Arg404Trp
|
|
NM_001171088.3:c.1078C>T
(CLCN2)
|
NP_001164559.1:p.Arg360Trp
|
|
NM_001171089.3:c.1210C>T
(CLCN2)
|
NP_001164560.1:p.Arg404Trp
|
|