|
ENST00000265593.9:c.1135T=
(CLCN2)
MANE Select
|
ENSP00000265593.4:p.Phe379=
|
|
|
ENST00000475279.2:c.517T=
(CLCN2)
|
|
|
|
ENST00000636180.1:c.*111T=
(CLCN2)
|
ENSP00000490374.1:n.*111T=
|
|
|
ENST00000636241.1:c.1026T=
(CLCN2)
|
|
|
|
ENST00000636492.1:c.1018T=
(CLCN2)
|
ENSP00000490313.1:p.Phe340=
|
|
|
ENST00000636658.1:c.396T=
(CLCN2)
|
|
|
|
ENST00000636661.1:c.*1325T=
(CLCN2)
|
ENSP00000490764.1:n.*1325T=
|
|
|
ENST00000637392.1:n.2247T=
(CLCN2)
|
|
|
|
ENST00000637538.1:c.441T=
(CLCN2)
|
|
|
|
ENST00000637909.1:c.941T=
(CLCN2)
|
|
|
|
ENST00000638134.1:c.943T=
(CLCN2)
|
|
|
|
ENST00000265593.8:c.1135T=
(CLCN2)
|
ENSP00000265593.4:p.Phe379=
|
|
|
ENST00000344937.11:c.1135T=
(CLCN2)
|
ENSP00000345056.7:p.Phe379=
|
|
|
ENST00000430397.5:c.78T=
(CLCN2)
|
|
|
|
ENST00000434054.6:c.1003T=
(CLCN2)
|
ENSP00000400425.2:p.Phe335=
|
|
|
ENST00000444495.1:c.2106+211022A=
(EIF2B5)
|
ENSP00000409142.1:n.2106+211022A=
|
|
|
ENST00000457512.1:c.1135T=
(CLCN2)
|
ENSP00000391928.1:p.Phe379=
|
|
|
ENST00000475279.1:n.153T=
(CLCN2)
|
|
|
|
ENST00000485667.1:n.1142T=
(CLCN2)
|
|
|
|
NM_001171087.2:c.1135T=
(CLCN2)
|
NP_001164558.1:p.Phe379=
|
|
|
NM_001171088.2:c.1003T=
(CLCN2)
|
NP_001164559.1:p.Phe335=
|
|
|
NM_001171089.2:c.1135T=
(CLCN2)
|
NP_001164560.1:p.Phe379=
|
|
|
NM_004366.5:c.1135T=
(CLCN2)
|
NP_004357.3:p.Phe379=
|
|
|
XM_006713489.1:c.1135T=
(CLCN2)
|
XP_006713552.1:p.Phe379=
|
|
|
XM_006713490.1:c.-24T=
(CLCN2)
|
XP_006713553.1:n.-24T=
|
|
|
XM_011512401.1:c.1135T=
(CLCN2)
|
XP_011510703.1:p.Phe379=
|
|
|
XM_011512402.1:c.1135T=
(CLCN2)
|
XP_011510704.1:p.Phe379=
|
|
|
XM_006713490.2:c.-24T=
(CLCN2)
|
XP_006713553.1:n.-24T=
|
|
|
XR_001740001.1:n.1259T=
(CLCN2)
|
|
|
|
XR_001740002.1:n.1259T=
(CLCN2)
|
|
|
|
NM_004366.6:c.1135T=
(CLCN2)
MANE Select
|
NP_004357.3:p.Phe379=
|
|
|
NM_001171087.3:c.1135T=
(CLCN2)
|
NP_001164558.1:p.Phe379=
|
|
|
NM_001171088.3:c.1003T=
(CLCN2)
|
NP_001164559.1:p.Phe335=
|
|
|
NM_001171089.3:c.1135T=
(CLCN2)
|
NP_001164560.1:p.Phe379=
|
|
