ENST00000703570.1:n.2844+1330G>A
(CARD14)
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ENST00000326317.11:c.1373C>T
(SGSH)
MANE Select
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ENSP00000314606.6:p.Ala458Val
|
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ENST00000326317.10:c.1373C>T
(SGSH)
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ENSP00000314606.6:p.Ala458Val
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ENST00000572257.5:c.551+1483C>T
(SGSH)
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ENST00000573150.5:c.*583C>T
(SGSH)
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ENSP00000459280.1:n.*583C>T
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ENST00000575282.5:n.4256C>T
(SGSH)
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ENST00000576856.1:c.627C>T
(SGSH)
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ENSP00000460720.1:n.627C>T
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NM_000199.3:c.1373C>T
(SGSH)
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NP_000190.1:p.Ala458Val
|
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XM_005257583.3:c.949+1483C>T
(SGSH)
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XP_005257640.1:n.949+1483C>T
|
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NM_000199.4:c.1373C>T
(SGSH)
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NP_000190.1:p.Ala458Val
|
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NM_001352921.1:c.*460C>T
(SGSH)
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NP_001339850.1:n.*460C>T
|
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NM_001352922.1:c.*423C>T
(SGSH)
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NP_001339851.1:n.*423C>T
|
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NR_148201.1:n.1354C>T
(SGSH)
|
|
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XM_005257583.4:c.949+1483C>T
(SGSH)
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XP_005257640.1:n.949+1483C>T
|
|
XM_017024952.1:c.*1277C>T
(SGSH)
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XP_016880441.1:n.*1277C>T
|
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XR_001752585.1:n.1393C>T
(SGSH)
|
|
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XR_001752586.1:n.969+1483C>T
(SGSH)
|
|
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XR_001752587.1:n.969+1483C>T
(SGSH)
|
|
|
XR_001752588.1:n.969+1483C>T
(SGSH)
|
|
|
XR_001752589.1:n.969+1483C>T
(SGSH)
|
|
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XR_001752590.1:n.969+1483C>T
(SGSH)
|
|
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XR_001752591.1:n.969+1483C>T
(SGSH)
|
|
|
XR_001752592.1:n.969+1483C>T
(SGSH)
|
|
|
XR_002958057.1:n.1024+1281C>T
(SGSH)
|
|
|
NM_000199.5:c.1373C>T
(SGSH)
MANE Select
|
NP_000190.1:p.Ala458Val
|
|
NM_001352921.2:c.*460C>T
(SGSH)
|
NP_001339850.1:n.*460C>T
|
|
NM_001352922.2:c.*423C>T
(SGSH)
|
NP_001339851.1:n.*423C>T
|
|
NR_148201.2:n.1287C>T
(SGSH)
|
|
|
NM_001352921.3:c.*460C>T
(SGSH)
|
NP_001339850.1:n.*460C>T
|
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