ENST00000703570.1:n.2845-2010T>G
(CARD14)
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ENST00000326317.11:c.693A>C
(SGSH)
MANE Select
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ENSP00000314606.6:p.Ala231=
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ENST00000326317.10:c.693A>C
(SGSH)
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ENSP00000314606.6:p.Ala231=
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ENST00000570923.1:c.728A>C
(SGSH)
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ENSP00000458200.1:p.Gln243Pro
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ENST00000572208.5:n.560A>C
(SGSH)
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ENST00000572257.5:c.295A>C
(SGSH)
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ENST00000573150.5:c.587A>C
(SGSH)
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ENSP00000459280.1:p.Gln196Pro
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ENST00000574505.5:c.552A>C
(SGSH)
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ENST00000575282.5:n.988A>C
(SGSH)
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ENST00000576941.5:c.*109A>C
(SGSH)
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ENSP00000461160.1:n.*109A>C
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NM_000199.3:c.693A>C
(SGSH)
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NP_000190.1:p.Ala231=
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XM_005257582.2:c.693A>C
(SGSH)
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XP_005257639.1:p.Ala231=
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XM_005257583.3:c.693A>C
(SGSH)
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XP_005257640.1:p.Ala231=
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XM_011525126.1:c.693A>C
(SGSH)
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XP_011523428.1:p.Ala231=
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XM_011525127.1:c.693A>C
(SGSH)
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XP_011523429.1:p.Ala231=
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XR_934532.1:n.713A>C
(SGSH)
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NM_000199.4:c.693A>C
(SGSH)
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NP_000190.1:p.Ala231=
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NM_001352921.1:c.693A>C
(SGSH)
|
NP_001339850.1:p.Ala231=
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NM_001352922.1:c.693A>C
(SGSH)
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NP_001339851.1:p.Ala231=
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NR_148201.1:n.674A>C
(SGSH)
|
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XM_005257583.4:c.693A>C
(SGSH)
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XP_005257640.1:p.Ala231=
|
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XM_017024952.1:c.693A>C
(SGSH)
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XP_016880441.1:p.Ala231=
|
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XR_001752585.1:n.713A>C
(SGSH)
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XR_001752586.1:n.713A>C
(SGSH)
|
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XR_001752587.1:n.713A>C
(SGSH)
|
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XR_001752588.1:n.713A>C
(SGSH)
|
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XR_001752589.1:n.713A>C
(SGSH)
|
|
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XR_001752590.1:n.713A>C
(SGSH)
|
|
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XR_001752591.1:n.713A>C
(SGSH)
|
|
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XR_001752592.1:n.713A>C
(SGSH)
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XR_002958057.1:n.713A>C
(SGSH)
|
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XR_934532.2:n.713A>C
(SGSH)
|
|
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NM_000199.5:c.693A>C
(SGSH)
MANE Select
|
NP_000190.1:p.Ala231=
|
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NM_001352921.2:c.693A>C
(SGSH)
|
NP_001339850.1:p.Ala231=
|
|
NM_001352922.2:c.693A>C
(SGSH)
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NP_001339851.1:p.Ala231=
|
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NR_148201.2:n.607A>C
(SGSH)
|
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NM_001352921.3:c.693A>C
(SGSH)
|
NP_001339850.1:p.Ala231=
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