ENST00000703570.1:n.2844+1185C>A
(CARD14)
|
|
|
ENST00000326317.11:c.*9G>T
(SGSH)
MANE Select
|
ENSP00000314606.6:n.*9G>T
|
|
ENST00000326317.10:c.*9G>T
(SGSH)
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ENSP00000314606.6:n.*9G>T
|
|
ENST00000572257.5:c.551+1628G>T
(SGSH)
|
|
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ENST00000573150.5:c.*728G>T
(SGSH)
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ENSP00000459280.1:n.*728G>T
|
|
ENST00000575282.5:n.4401G>T
(SGSH)
|
|
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ENST00000576856.1:c.772G>T
(SGSH)
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ENSP00000460720.1:n.772G>T
|
|
NM_000199.3:c.*9G>T
(SGSH)
|
NP_000190.1:n.*9G>T
|
|
XM_005257583.3:c.949+1628G>T
(SGSH)
|
XP_005257640.1:n.949+1628G>T
|
|
NM_000199.4:c.*9G>T
(SGSH)
|
NP_000190.1:n.*9G>T
|
|
NM_001352921.1:c.*605G>T
(SGSH)
|
NP_001339850.1:n.*605G>T
|
|
NM_001352922.1:c.*568G>T
(SGSH)
|
NP_001339851.1:n.*568G>T
|
|
NR_148201.1:n.1499G>T
(SGSH)
|
|
|
XM_005257583.4:c.949+1628G>T
(SGSH)
|
XP_005257640.1:n.949+1628G>T
|
|
XM_017024952.1:c.*1422G>T
(SGSH)
|
XP_016880441.1:n.*1422G>T
|
|
XR_001752585.1:n.1538G>T
(SGSH)
|
|
|
XR_001752586.1:n.969+1628G>T
(SGSH)
|
|
|
XR_001752587.1:n.969+1628G>T
(SGSH)
|
|
|
XR_001752588.1:n.969+1628G>T
(SGSH)
|
|
|
XR_001752589.1:n.969+1628G>T
(SGSH)
|
|
|
XR_001752590.1:n.969+1628G>T
(SGSH)
|
|
|
XR_001752591.1:n.969+1628G>T
(SGSH)
|
|
|
XR_001752592.1:n.969+1628G>T
(SGSH)
|
|
|
XR_002958057.1:n.1024+1426G>T
(SGSH)
|
|
|
NM_000199.5:c.*9G>T
(SGSH)
MANE Select
|
NP_000190.1:n.*9G>T
|
|
NM_001352921.2:c.*605G>T
(SGSH)
|
NP_001339850.1:n.*605G>T
|
|
NM_001352922.2:c.*568G>T
(SGSH)
|
NP_001339851.1:n.*568G>T
|
|
NR_148201.2:n.1432G>T
(SGSH)
|
|
|
NM_001352921.3:c.*605G>T
(SGSH)
|
NP_001339850.1:n.*605G>T
|
|