ENST00000426263.10:c.427T>G
MANE Select
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ENSP00000416293.2:p.Tyr143Asp
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ENST00000674765.1:c.427T>G
|
ENSP00000501811.1:p.Tyr143Asp
|
|
ENST00000675112.1:n.450T>G
|
|
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ENST00000676254.1:n.876T>G
|
|
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ENST00000372500.4:c.331T>G
|
ENSP00000361578.4:p.Tyr111Asp
|
|
ENST00000426263.7:c.427T>G
|
ENSP00000416293.2:p.Tyr143Asp
|
|
ENST00000439722.2:c.306T>G
|
ENSP00000395521.2:n.306T>G
|
|
ENST00000475162.3:c.326T>G
|
|
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ENST00000625233.2:n.635T>G
|
|
|
ENST00000630287.2:c.427T>G
|
ENSP00000486694.1:p.Tyr143Asp
|
|
NM_006516.2:c.427T>G
|
NP_006507.2:p.Tyr143Asp
|
|
NM_006516.3:c.427T>G
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NP_006507.2:p.Tyr143Asp
|
|
NM_006516.4:c.427T>G
MANE Select
|
NP_006507.2:p.Tyr143Asp
|
|