ENST00000426263.10:c.827T>A
MANE Select
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ENSP00000416293.2:p.Val276Glu
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ENST00000674765.1:c.827T>A
|
ENSP00000501811.1:p.Val276Glu
|
|
ENST00000675112.1:n.850T>A
|
|
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ENST00000676254.1:n.1276T>A
|
|
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ENST00000426263.7:c.827T>A
|
ENSP00000416293.2:p.Val276Glu
|
|
ENST00000439722.2:c.706T>A
|
ENSP00000395521.2:n.706T>A
|
|
ENST00000475162.3:c.415+993T>A
|
|
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ENST00000630287.2:c.*142T>A
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ENSP00000486694.1:n.*142T>A
|
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NM_006516.2:c.827T>A
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NP_006507.2:p.Val276Glu
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NM_006516.3:c.827T>A
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NP_006507.2:p.Val276Glu
|
|
NM_006516.4:c.827T>A
MANE Select
|
NP_006507.2:p.Val276Glu
|
|