ENST00000426263.10:c.663G>A
MANE Select
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ENSP00000416293.2:p.Glu221=
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ENST00000669445.1:c.40G>A
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ENST00000674765.1:c.663G>A
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ENSP00000501811.1:p.Glu221=
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ENST00000675112.1:n.686G>A
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|
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ENST00000676254.1:n.1112G>A
|
|
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ENST00000426263.7:c.663G>A
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ENSP00000416293.2:p.Glu221=
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ENST00000439722.2:c.542G>A
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ENSP00000395521.2:n.542G>A
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ENST00000475162.3:c.415+737G>A
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ENST00000630287.2:c.517-109G>A
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ENSP00000486694.1:n.517-109G>A
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NM_006516.2:c.663G>A
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NP_006507.2:p.Glu221=
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NM_006516.3:c.663G>A
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NP_006507.2:p.Glu221=
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NM_006516.4:c.663G>A
MANE Select
|
NP_006507.2:p.Glu221=
|
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