ENST00000367698.4:c.878G>A
MANE Select
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ENSP00000356671.3:p.Arg293Gln
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ENST00000367698.3:c.878G>A
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ENSP00000356671.3:p.Arg293Gln
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ENST00000487183.1:n.529G>A
|
|
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ENST00000617423.4:c.559+2037G>A
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ENSP00000478688.1:n.559+2037G>A
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NM_000488.3:c.878G>A , LRG_577t1:c.878G>A
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NP_000479.1:p.Arg293Gln
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XM_005245198.2:c.734G>A
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XP_005245255.1:p.Arg245Gln
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NM_001365052.1:c.734G>A
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NP_001351981.1:p.Arg245Gln
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NM_000488.4:c.878G>A
MANE Select
|
NP_000479.1:p.Arg293Gln
|
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NM_001365052.2:c.734G>A
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NP_001351981.1:p.Arg245Gln
|
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NM_001386302.1:c.1001G>A
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NP_001373231.1:p.Arg334Gln
|
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NM_001386303.1:c.959G>A
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NP_001373232.1:p.Arg320Gln
|
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NM_001386304.1:c.857G>A
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NP_001373233.1:p.Arg286Gln
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NM_001386305.1:c.821G>A
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NP_001373234.1:p.Arg274Gln
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NM_001386306.1:c.662G>A
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NP_001373235.1:p.Arg221Gln
|
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