ENST00000426263.10:c.680T>A
MANE Select
|
ENSP00000416293.2:p.Val227Glu
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ENST00000669445.1:c.57-47T>A
|
|
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ENST00000674765.1:c.680T>A
|
ENSP00000501811.1:p.Val227Glu
|
|
ENST00000675112.1:n.703T>A
|
|
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ENST00000676254.1:n.1129T>A
|
|
|
ENST00000426263.7:c.680T>A
|
ENSP00000416293.2:p.Val227Glu
|
|
ENST00000439722.2:c.559T>A
|
ENSP00000395521.2:n.559T>A
|
|
ENST00000475162.3:c.415+846T>A
|
|
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ENST00000630287.2:c.517T>A
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ENSP00000486694.1:p.Cys173Ser
|
|
NM_006516.2:c.680T>A
|
NP_006507.2:p.Val227Glu
|
|
NM_006516.3:c.680T>A
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NP_006507.2:p.Val227Glu
|
|
NM_006516.4:c.680T>A
MANE Select
|
NP_006507.2:p.Val227Glu
|
|