ENST00000280871.9:c.926-8766C>T
MANE Select
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ENSP00000280871.4:n.926-8766C>T
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ENST00000280871.8:c.926-8766C>T
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ENSP00000280871.4:n.926-8766C>T
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|
ENST00000380858.1:c.926-8766C>T
|
ENSP00000370239.1:n.926-8766C>T
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NM_052885.3:c.926-8766C>T
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NP_443117.3:n.926-8766C>T
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XM_011537847.1:c.926-8766C>T
|
XP_011536149.1:n.926-8766C>T
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XM_011537848.1:c.926-8766C>T
|
XP_011536150.1:n.926-8766C>T
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XM_011537849.1:c.926-8766C>T
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XP_011536151.1:n.926-8766C>T
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XM_011537850.1:c.926-8766C>T
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XP_011536152.1:n.926-8766C>T
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XM_011537847.2:c.926-8766C>T
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XP_011536149.1:n.926-8766C>T
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XM_011537849.2:c.926-8766C>T
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XP_011536151.1:n.926-8766C>T
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XM_011537850.3:c.926-8766C>T
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XP_011536152.1:n.926-8766C>T
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XM_017018764.1:c.359-8766C>T
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XP_016874253.1:n.359-8766C>T
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XM_017018765.1:c.359-8766C>T
|
XP_016874254.1:n.359-8766C>T
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XM_017018766.1:c.206-8766C>T
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XP_016874255.1:n.206-8766C>T
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XR_001748567.2:n.1203-8766C>T
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XR_001748568.1:n.1203-8766C>T
|
|
|
NM_052885.4:c.926-8766C>T
MANE Select
|
NP_443117.3:n.926-8766C>T
|
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