ENST00000703570.1:n.2845-1165C>T
(CARD14)
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ENST00000326317.11:c.420G>A
(SGSH)
MANE Select
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ENSP00000314606.6:p.Glu140=
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ENST00000326317.10:c.420G>A
(SGSH)
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ENSP00000314606.6:p.Glu140=
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ENST00000570427.1:c.438G>A
(SGSH)
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ENSP00000459765.1:p.Glu146=
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ENST00000570923.1:c.455G>A
(SGSH)
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ENSP00000458200.1:p.Arg152Lys
|
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ENST00000571051.5:n.375+332G>A
(SGSH)
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ENST00000571675.5:n.440G>A
(SGSH)
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ENST00000572208.5:n.373+332G>A
(SGSH)
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ENST00000572257.5:c.22G>A
(SGSH)
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ENST00000573150.5:c.314G>A
(SGSH)
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ENSP00000459280.1:p.Arg105Lys
|
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ENST00000574505.5:c.301-22G>A
(SGSH)
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ENST00000575282.5:n.429G>A
(SGSH)
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ENST00000576707.5:c.159G>A
(SGSH)
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ENSP00000461128.1:p.Glu53=
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ENST00000576941.5:c.250-373G>A
(SGSH)
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ENSP00000461160.1:n.250-373G>A
|
|
NM_000199.3:c.420G>A
(SGSH)
|
NP_000190.1:p.Glu140=
|
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XM_005257582.2:c.420G>A
(SGSH)
|
XP_005257639.1:p.Glu140=
|
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XM_005257583.3:c.420G>A
(SGSH)
|
XP_005257640.1:p.Glu140=
|
|
XM_011525126.1:c.420G>A
(SGSH)
|
XP_011523428.1:p.Glu140=
|
|
XM_011525127.1:c.420G>A
(SGSH)
|
XP_011523429.1:p.Glu140=
|
|
XR_934532.1:n.440G>A
(SGSH)
|
|
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NM_000199.4:c.420G>A
(SGSH)
|
NP_000190.1:p.Glu140=
|
|
NM_001352921.1:c.420G>A
(SGSH)
|
NP_001339850.1:p.Glu140=
|
|
NM_001352922.1:c.420G>A
(SGSH)
|
NP_001339851.1:p.Glu140=
|
|
NR_148201.1:n.401G>A
(SGSH)
|
|
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XM_005257583.4:c.420G>A
(SGSH)
|
XP_005257640.1:p.Glu140=
|
|
XM_017024952.1:c.420G>A
(SGSH)
|
XP_016880441.1:p.Glu140=
|
|
XR_001752585.1:n.440G>A
(SGSH)
|
|
|
XR_001752586.1:n.440G>A
(SGSH)
|
|
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XR_001752587.1:n.440G>A
(SGSH)
|
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XR_001752588.1:n.440G>A
(SGSH)
|
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XR_001752589.1:n.440G>A
(SGSH)
|
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XR_001752590.1:n.440G>A
(SGSH)
|
|
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XR_001752591.1:n.440G>A
(SGSH)
|
|
|
XR_001752592.1:n.440G>A
(SGSH)
|
|
|
XR_002958057.1:n.440G>A
(SGSH)
|
|
|
XR_934532.2:n.440G>A
(SGSH)
|
|
|
NM_000199.5:c.420G>A
(SGSH)
MANE Select
|
NP_000190.1:p.Glu140=
|
|
NM_001352921.2:c.420G>A
(SGSH)
|
NP_001339850.1:p.Glu140=
|
|
NM_001352922.2:c.420G>A
(SGSH)
|
NP_001339851.1:p.Glu140=
|
|
NR_148201.2:n.334G>A
(SGSH)
|
|
|
NM_001352921.3:c.420G>A
(SGSH)
|
NP_001339850.1:p.Glu140=
|
|