ENST00000455537.7:c.2911T>A
MANE Select
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ENSP00000408979.2:p.Phe971Ile
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ENST00000674619.1:c.2932T>A
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ENSP00000502270.1:p.Phe978Ile
|
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ENST00000675697.1:c.2T>A
|
|
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ENST00000675737.1:n.315T>A
|
|
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ENST00000675882.1:n.2434T>A
|
|
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ENST00000675929.1:n.1469T>A
|
|
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ENST00000676055.1:c.2T>A
|
|
|
ENST00000676457.1:c.2806T>A
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ENSP00000501588.1:p.Phe936Ile
|
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ENST00000286452.5:c.2644T>A
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ENSP00000286452.5:p.Phe882Ile
|
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ENST00000455537.6:c.2911T>A
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ENSP00000408979.2:p.Phe971Ile
|
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ENST00000552227.1:n.194T>A
|
|
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NM_004984.2:c.2911T>A
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NP_004975.2:p.Phe971Ile
|
|
NM_001354705.1:c.2644T>A
|
NP_001341634.1:p.Phe882Ile
|
|
NM_004984.3:c.2911T>A
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NP_004975.2:p.Phe971Ile
|
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XR_002957324.1:n.3144T>A
|
|
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NM_004984.4:c.2911T>A
MANE Select
|
NP_004975.2:p.Phe971Ile
|
|
NM_001354705.2:c.2644T>A
|
NP_001341634.1:p.Phe882Ile
|
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