ENST00000367698.4:c.963G>A
MANE Select
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ENSP00000356671.3:p.Glu321=
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ENST00000367698.3:c.963G>A
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ENSP00000356671.3:p.Glu321=
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ENST00000487183.1:n.614G>A
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|
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ENST00000617423.4:c.559+2122G>A
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ENSP00000478688.1:n.559+2122G>A
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NM_000488.3:c.963G>A , LRG_577t1:c.963G>A
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NP_000479.1:p.Glu321=
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XM_005245198.2:c.819G>A
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XP_005245255.1:p.Glu273=
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NM_001365052.1:c.819G>A
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NP_001351981.1:p.Glu273=
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NM_000488.4:c.963G>A
MANE Select
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NP_000479.1:p.Glu321=
|
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NM_001365052.2:c.819G>A
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NP_001351981.1:p.Glu273=
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NM_001386302.1:c.1086G>A
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NP_001373231.1:p.Glu362=
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NM_001386303.1:c.1044G>A
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NP_001373232.1:p.Glu348=
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NM_001386304.1:c.942G>A
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NP_001373233.1:p.Glu314=
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NM_001386305.1:c.906G>A
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NP_001373234.1:p.Glu302=
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NM_001386306.1:c.747G>A
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NP_001373235.1:p.Glu249=
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