ENST00000369538.4:c.389A>C
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ENSP00000358551.4:p.Glu130Ala
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ENST00000520113.7:c.401A>C
MANE Select
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ENSP00000430075.3:p.Glu134Ala
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ENST00000637080.1:c.404A>C
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ENSP00000489753.1:p.Glu135Ala
|
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ENST00000639077.1:n.66A>C
|
|
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ENST00000369538.3:c.488A>C
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ENSP00000358551.3:p.Glu163Ala
|
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ENST00000485564.3:n.275A>C
|
|
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ENST00000520113.6:c.500A>C
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ENSP00000430075.2:p.Glu167Ala
|
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NM_000036.2:c.500A>C
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NP_000027.2:p.Glu167Ala
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NM_001172626.1:c.488A>C
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NP_001166097.1:p.Glu163Ala
|
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NM_000036.3:c.401A>C
MANE Select
|
NP_000027.3:p.Glu134Ala
|
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NM_001172626.2:c.389A>C
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NP_001166097.2:p.Glu130Ala
|
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