|
ENST00000703570.1:n.2845-1983C>G
(CARD14)
|
|
|
|
ENST00000326317.11:c.666G>C
(SGSH)
MANE Select
|
ENSP00000314606.6:p.Val222=
|
|
|
ENST00000326317.10:c.666G>C
(SGSH)
|
ENSP00000314606.6:p.Val222=
|
|
|
ENST00000570923.1:c.701G>C
(SGSH)
|
ENSP00000458200.1:p.Cys234Ser
|
|
|
ENST00000572208.5:n.533G>C
(SGSH)
|
|
|
|
ENST00000572257.5:c.268G>C
(SGSH)
|
|
|
|
ENST00000573150.5:c.560G>C
(SGSH)
|
ENSP00000459280.1:p.Cys187Ser
|
|
|
ENST00000574505.5:c.525G>C
(SGSH)
|
|
|
|
ENST00000575282.5:n.961G>C
(SGSH)
|
|
|
|
ENST00000576941.5:c.*82G>C
(SGSH)
|
ENSP00000461160.1:n.*82G>C
|
|
|
NM_000199.3:c.666G>C
(SGSH)
|
NP_000190.1:p.Val222=
|
|
|
XM_005257582.2:c.666G>C
(SGSH)
|
XP_005257639.1:p.Val222=
|
|
|
XM_005257583.3:c.666G>C
(SGSH)
|
XP_005257640.1:p.Val222=
|
|
|
XM_011525126.1:c.666G>C
(SGSH)
|
XP_011523428.1:p.Val222=
|
|
|
XM_011525127.1:c.666G>C
(SGSH)
|
XP_011523429.1:p.Val222=
|
|
|
XR_934532.1:n.686G>C
(SGSH)
|
|
|
|
NM_000199.4:c.666G>C
(SGSH)
|
NP_000190.1:p.Val222=
|
|
|
NM_001352921.1:c.666G>C
(SGSH)
|
NP_001339850.1:p.Val222=
|
|
|
NM_001352922.1:c.666G>C
(SGSH)
|
NP_001339851.1:p.Val222=
|
|
|
NR_148201.1:n.647G>C
(SGSH)
|
|
|
|
XM_005257583.4:c.666G>C
(SGSH)
|
XP_005257640.1:p.Val222=
|
|
|
XM_017024952.1:c.666G>C
(SGSH)
|
XP_016880441.1:p.Val222=
|
|
|
XR_001752585.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752586.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752587.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752588.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752589.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752590.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752591.1:n.686G>C
(SGSH)
|
|
|
|
XR_001752592.1:n.686G>C
(SGSH)
|
|
|
|
XR_002958057.1:n.686G>C
(SGSH)
|
|
|
|
XR_934532.2:n.686G>C
(SGSH)
|
|
|
|
NM_000199.5:c.666G>C
(SGSH)
MANE Select
|
NP_000190.1:p.Val222=
|
|
|
NM_001352921.2:c.666G>C
(SGSH)
|
NP_001339850.1:p.Val222=
|
|
|
NM_001352922.2:c.666G>C
(SGSH)
|
NP_001339851.1:p.Val222=
|
|
|
NR_148201.2:n.580G>C
(SGSH)
|
|
|
|
NM_001352921.3:c.666G>C
(SGSH)
|
NP_001339850.1:p.Val222=
|
|
