ENST00000367698.4:c.821C>A
MANE Select
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ENSP00000356671.3:p.Ala274Asp
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|
ENST00000367698.3:c.821C>A
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ENSP00000356671.3:p.Ala274Asp
|
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ENST00000487183.1:n.472C>A
|
|
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ENST00000617423.4:c.559+1980C>A
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ENSP00000478688.1:n.559+1980C>A
|
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NM_000488.3:c.821C>A , LRG_577t1:c.821C>A
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NP_000479.1:p.Ala274Asp
|
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XM_005245198.2:c.677C>A
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XP_005245255.1:p.Ala226Asp
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NM_001365052.1:c.677C>A
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NP_001351981.1:p.Ala226Asp
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NM_000488.4:c.821C>A
MANE Select
|
NP_000479.1:p.Ala274Asp
|
|
NM_001365052.2:c.677C>A
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NP_001351981.1:p.Ala226Asp
|
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NM_001386302.1:c.944C>A
|
NP_001373231.1:p.Ala315Asp
|
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NM_001386303.1:c.902C>A
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NP_001373232.1:p.Ala301Asp
|
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NM_001386304.1:c.800C>A
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NP_001373233.1:p.Ala267Asp
|
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NM_001386305.1:c.764C>A
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NP_001373234.1:p.Ala255Asp
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NM_001386306.1:c.605C>A
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NP_001373235.1:p.Ala202Asp
|
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