ENST00000703570.1:n.2844+2700A>G
(CARD14)
|
|
|
ENST00000326317.11:c.949+113T>C
(SGSH)
MANE Select
|
ENSP00000314606.6:n.949+113T>C
|
|
ENST00000326317.10:c.949+113T>C
(SGSH)
|
ENSP00000314606.6:n.949+113T>C
|
|
ENST00000570923.1:c.*272T>C
(SGSH)
|
ENSP00000458200.1:n.*272T>C
|
|
ENST00000572257.5:c.551+113T>C
(SGSH)
|
|
|
ENST00000573150.5:c.*159+113T>C
(SGSH)
|
ENSP00000459280.1:n.*159+113T>C
|
|
ENST00000575282.5:n.2886T>C
(SGSH)
|
|
|
ENST00000576856.1:c.149-35T>C
(SGSH)
|
ENSP00000460720.1:n.149-35T>C
|
|
NM_000199.3:c.949+113T>C
(SGSH)
|
NP_000190.1:n.949+113T>C
|
|
XM_005257582.2:c.949+113T>C
(SGSH)
|
XP_005257639.1:n.949+113T>C
|
|
XM_005257583.3:c.949+113T>C
(SGSH)
|
XP_005257640.1:n.949+113T>C
|
|
XM_011525126.1:c.950-35T>C
(SGSH)
|
XP_011523428.1:n.950-35T>C
|
|
XM_011525127.1:c.950-35T>C
(SGSH)
|
XP_011523429.1:n.950-35T>C
|
|
XR_934532.1:n.1082T>C
(SGSH)
|
|
|
NM_000199.4:c.949+113T>C
(SGSH)
|
NP_000190.1:n.949+113T>C
|
|
NM_001352921.1:c.949+113T>C
(SGSH)
|
NP_001339850.1:n.949+113T>C
|
|
NM_001352922.1:c.950-35T>C
(SGSH)
|
NP_001339851.1:n.950-35T>C
|
|
NR_148201.1:n.930+113T>C
(SGSH)
|
|
|
XM_005257583.4:c.949+113T>C
(SGSH)
|
XP_005257640.1:n.949+113T>C
|
|
XM_017024952.1:c.950-35T>C
(SGSH)
|
XP_016880441.1:n.950-35T>C
|
|
XR_001752585.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752586.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752587.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752588.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752589.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752590.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752591.1:n.969+113T>C
(SGSH)
|
|
|
XR_001752592.1:n.969+113T>C
(SGSH)
|
|
|
XR_002958057.1:n.970-35T>C
(SGSH)
|
|
|
XR_934532.2:n.1082T>C
(SGSH)
|
|
|
NM_000199.5:c.949+113T>C
(SGSH)
MANE Select
|
NP_000190.1:n.949+113T>C
|
|
NM_001352921.2:c.949+113T>C
(SGSH)
|
NP_001339850.1:n.949+113T>C
|
|
NM_001352922.2:c.950-35T>C
(SGSH)
|
NP_001339851.1:n.950-35T>C
|
|
NR_148201.2:n.863+113T>C
(SGSH)
|
|
|
NM_001352921.3:c.949+113T>C
(SGSH)
|
NP_001339850.1:n.949+113T>C
|
|