ENST00000321612.8:c.2031T>A
MANE Select
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ENSP00000370737.4:p.Asp677Glu
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ENST00000460457.2:n.191T>A
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ENST00000638233.1:n.466T>A
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ENST00000638661.1:c.231T>A
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ENSP00000491369.1:p.Asp77Glu
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ENST00000638694.1:n.218T>A
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|
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ENST00000639318.1:c.231T>A
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ENSP00000491932.1:p.Asp77Glu
|
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ENST00000639364.1:n.1731T>A
|
|
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ENST00000639443.1:n.1599T>A
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|
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ENST00000639954.1:n.1739T>A
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|
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ENST00000640208.1:c.231T>A
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ENSP00000491895.1:p.Asp77Glu
|
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ENST00000640505.1:n.270T>A
|
|
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ENST00000640592.1:n.1914T>A
|
|
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ENST00000321612.6:c.2031T>A
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ENSP00000370737.3:p.Asp677Glu
|
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ENST00000460457.1:n.170T>A
|
|
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NM_000170.2:c.2031T>A , LRG_643t1:c.2031T>A
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NP_000161.2:p.Asp677Glu
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NM_000170.3:c.2031T>A
MANE Select
|
NP_000161.2:p.Asp677Glu
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