ENST00000262027.10:c.1385A>C
MANE Select
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ENSP00000262027.5:p.Glu462Ala
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ENST00000262027.9:c.1385A>C
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ENSP00000262027.5:p.Glu462Ala
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ENST00000447721.6:n.1027A>C
|
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ENST00000537638.6:c.1385A>C
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ENSP00000446168.2:p.Glu462Ala
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ENST00000545888.6:c.*886A>C
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ENSP00000439307.2:n.*886A>C
|
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ENST00000546971.5:n.129A>C
|
|
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ENST00000548944.1:c.134-4781A>C
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ENSP00000449071.1:n.134-4781A>C
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ENST00000549603.1:n.331A>C
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ENST00000628866.2:c.*886A>C
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ENSP00000486738.1:n.*886A>C
|
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NM_004990.3:c.1385A>C
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NP_004981.2:p.Glu462Ala
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XM_006719398.2:c.683A>C
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XP_006719461.1:p.Glu228Ala
|
|
XM_011538353.1:c.1385A>C
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XP_011536655.1:p.Glu462Ala
|
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XM_006719398.4:c.683A>C
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XP_006719461.1:p.Glu228Ala
|
|
XR_001748704.2:n.1408A>C
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|
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XR_002957327.1:n.1332A>C
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|
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NM_004990.4:c.1385A>C
MANE Select
|
NP_004981.2:p.Glu462Ala
|
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