ENST00000703570.1:n.2844+1393T>C
(CARD14)
|
|
|
ENST00000326317.11:c.1310A>G
(SGSH)
MANE Select
|
ENSP00000314606.6:p.Glu437Gly
|
|
ENST00000326317.10:c.1310A>G
(SGSH)
|
ENSP00000314606.6:p.Glu437Gly
|
|
ENST00000572257.5:c.551+1420A>G
(SGSH)
|
|
|
ENST00000573150.5:c.*520A>G
(SGSH)
|
ENSP00000459280.1:n.*520A>G
|
|
ENST00000575282.5:n.4193A>G
(SGSH)
|
|
|
ENST00000576856.1:c.564A>G
(SGSH)
|
ENSP00000460720.1:n.564A>G
|
|
NM_000199.3:c.1310A>G
(SGSH)
|
NP_000190.1:p.Glu437Gly
|
|
XM_005257583.3:c.949+1420A>G
(SGSH)
|
XP_005257640.1:n.949+1420A>G
|
|
NM_000199.4:c.1310A>G
(SGSH)
|
NP_000190.1:p.Glu437Gly
|
|
NM_001352921.1:c.*397A>G
(SGSH)
|
NP_001339850.1:n.*397A>G
|
|
NM_001352922.1:c.*360A>G
(SGSH)
|
NP_001339851.1:n.*360A>G
|
|
NR_148201.1:n.1291A>G
(SGSH)
|
|
|
XM_005257583.4:c.949+1420A>G
(SGSH)
|
XP_005257640.1:n.949+1420A>G
|
|
XM_017024952.1:c.*1214A>G
(SGSH)
|
XP_016880441.1:n.*1214A>G
|
|
XR_001752585.1:n.1330A>G
(SGSH)
|
|
|
XR_001752586.1:n.969+1420A>G
(SGSH)
|
|
|
XR_001752587.1:n.969+1420A>G
(SGSH)
|
|
|
XR_001752588.1:n.969+1420A>G
(SGSH)
|
|
|
XR_001752589.1:n.969+1420A>G
(SGSH)
|
|
|
XR_001752590.1:n.969+1420A>G
(SGSH)
|
|
|
XR_001752591.1:n.969+1420A>G
(SGSH)
|
|
|
XR_001752592.1:n.969+1420A>G
(SGSH)
|
|
|
XR_002958057.1:n.1024+1218A>G
(SGSH)
|
|
|
NM_000199.5:c.1310A>G
(SGSH)
MANE Select
|
NP_000190.1:p.Glu437Gly
|
|
NM_001352921.2:c.*397A>G
(SGSH)
|
NP_001339850.1:n.*397A>G
|
|
NM_001352922.2:c.*360A>G
(SGSH)
|
NP_001339851.1:n.*360A>G
|
|
NR_148201.2:n.1224A>G
(SGSH)
|
|
|
NM_001352921.3:c.*397A>G
(SGSH)
|
NP_001339850.1:n.*397A>G
|
|