|
ENST00000265593.9:c.1320C>A
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Leu440=
|
|
|
ENST00000475279.2:c.702C>A
(CLCN2)
|
|
|
|
ENST00000636180.1:c.*296C>A
(CLCN2)
|
ENSP00000490374.1:n.*296C>A
|
|
|
ENST00000636241.1:c.1211C>A
(CLCN2)
|
|
|
|
ENST00000636492.1:c.1203C>A
(CLCN2)
|
ENSP00000490313.1:p.Leu401=
|
|
|
ENST00000636658.1:c.581C>A
(CLCN2)
|
|
|
|
ENST00000636661.1:c.*1510C>A
(CLCN2)
|
ENSP00000490764.1:n.*1510C>A
|
|
|
ENST00000637392.1:n.2596C>A
(CLCN2)
|
|
|
|
ENST00000637538.1:c.626C>A
(CLCN2)
|
|
|
|
ENST00000637909.1:c.1126C>A
(CLCN2)
|
|
|
|
ENST00000638134.1:c.1128C>A
(CLCN2)
|
|
|
|
ENST00000265593.8:c.1320C>A
(CLCN2)
|
ENSP00000265593.4:p.Leu440=
|
|
|
ENST00000344937.11:c.1320C>A
(CLCN2)
|
ENSP00000345056.7:p.Leu440=
|
|
|
ENST00000430397.5:c.263C>A
(CLCN2)
|
|
|
|
ENST00000434054.6:c.1188C>A
(CLCN2)
|
ENSP00000400425.2:p.Leu396=
|
|
|
ENST00000444495.1:c.2106+210673G>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+210673G>T
|
|
|
ENST00000457512.1:c.1320C>A
(CLCN2)
|
ENSP00000391928.1:p.Leu440=
|
|
|
ENST00000485667.1:n.1327C>A
(CLCN2)
|
|
|
|
NM_001171087.2:c.1320C>A
(CLCN2)
|
NP_001164558.1:p.Leu440=
|
|
|
NM_001171088.2:c.1188C>A
(CLCN2)
|
NP_001164559.1:p.Leu396=
|
|
|
NM_001171089.2:c.1320C>A
(CLCN2)
|
NP_001164560.1:p.Leu440=
|
|
|
NM_004366.5:c.1320C>A
(CLCN2)
|
NP_004357.3:p.Leu440=
|
|
|
XM_006713489.1:c.1320C>A
(CLCN2)
|
XP_006713552.1:p.Leu440=
|
|
|
XM_006713490.1:c.162C>A
(CLCN2)
|
XP_006713553.1:p.Leu54=
|
|
|
XM_011512401.1:c.1320C>A
(CLCN2)
|
XP_011510703.1:p.Leu440=
|
|
|
XM_011512402.1:c.1320C>A
(CLCN2)
|
XP_011510704.1:p.Leu440=
|
|
|
XM_006713490.2:c.162C>A
(CLCN2)
|
XP_006713553.1:p.Leu54=
|
|
|
XR_001740001.1:n.1444C>A
(CLCN2)
|
|
|
|
XR_001740002.1:n.1444C>A
(CLCN2)
|
|
|
|
NM_004366.6:c.1320C>A
(CLCN2)
MANE Select
|
NP_004357.3:p.Leu440=
|
|
|
NM_001171087.3:c.1320C>A
(CLCN2)
|
NP_001164558.1:p.Leu440=
|
|
|
NM_001171088.3:c.1188C>A
(CLCN2)
|
NP_001164559.1:p.Leu396=
|
|
|
NM_001171089.3:c.1320C>A
(CLCN2)
|
NP_001164560.1:p.Leu440=
|
|
