ENST00000265593.9:c.1143del
(CLCN2)
MANE Select
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ENSP00000265593.4:p.Gly382AlafsTer?
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ENST00000475279.2:c.525del
(CLCN2)
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ENST00000636180.1:c.*119del
(CLCN2)
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ENSP00000490374.1:n.*119del
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ENST00000636241.1:c.1034del
(CLCN2)
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ENST00000636492.1:c.1026del
(CLCN2)
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ENSP00000490313.1:p.Gly343AlafsTer?
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ENST00000636658.1:c.404del
(CLCN2)
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ENST00000636661.1:c.*1333del
(CLCN2)
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ENSP00000490764.1:n.*1333del
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ENST00000637392.1:n.2255del
(CLCN2)
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ENST00000637538.1:c.449del
(CLCN2)
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ENST00000637909.1:c.949del
(CLCN2)
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ENST00000638134.1:c.951del
(CLCN2)
|
|
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ENST00000265593.8:c.1143del
(CLCN2)
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ENSP00000265593.4:p.Gly382AlafsTer?
|
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ENST00000344937.11:c.1143del
(CLCN2)
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ENSP00000345056.7:p.Gly382AlafsTer?
|
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ENST00000430397.5:c.86del
(CLCN2)
|
|
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ENST00000434054.6:c.1011del
(CLCN2)
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ENSP00000400425.2:p.Gly338AlafsTer?
|
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ENST00000444495.1:c.2106+211014del
(EIF2B5)
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ENSP00000409142.1:n.2106+211014del
|
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ENST00000457512.1:c.1143del
(CLCN2)
|
ENSP00000391928.1:p.Gly382AlafsTer?
|
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ENST00000475279.1:n.161del
(CLCN2)
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ENST00000485667.1:n.1150del
(CLCN2)
|
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NM_001171087.2:c.1143del
(CLCN2)
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NP_001164558.1:p.Gly382AlafsTer?
|
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NM_001171088.2:c.1011del
(CLCN2)
|
NP_001164559.1:p.Gly338AlafsTer?
|
|
NM_001171089.2:c.1143del
(CLCN2)
|
NP_001164560.1:p.Gly382AlafsTer?
|
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NM_004366.5:c.1143del
(CLCN2)
|
NP_004357.3:p.Gly382AlafsTer?
|
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XM_006713489.1:c.1143del
(CLCN2)
|
XP_006713552.1:p.Gly382AlafsTer?
|
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XM_006713490.1:c.-16del
(CLCN2)
|
XP_006713553.1:n.-16del
|
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XM_011512401.1:c.1143del
(CLCN2)
|
XP_011510703.1:p.Gly382AlafsTer?
|
|
XM_011512402.1:c.1143del
(CLCN2)
|
XP_011510704.1:p.Gly382AlafsTer?
|
|
XM_006713490.2:c.-16del
(CLCN2)
|
XP_006713553.1:n.-16del
|
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XR_001740001.1:n.1267del
(CLCN2)
|
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XR_001740002.1:n.1267del
(CLCN2)
|
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NM_004366.6:c.1143del
(CLCN2)
MANE Select
|
NP_004357.3:p.Gly382AlafsTer?
|
|
NM_001171087.3:c.1143del
(CLCN2)
|
NP_001164558.1:p.Gly382AlafsTer?
|
|
NM_001171088.3:c.1011del
(CLCN2)
|
NP_001164559.1:p.Gly338AlafsTer?
|
|
NM_001171089.3:c.1143del
(CLCN2)
|
NP_001164560.1:p.Gly382AlafsTer?
|
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