ENST00000367698.4:c.861A>C
MANE Select
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ENSP00000356671.3:p.Glu287Asp
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ENST00000367698.3:c.861A>C
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ENSP00000356671.3:p.Glu287Asp
|
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ENST00000487183.1:n.512A>C
|
|
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ENST00000617423.4:c.559+2020A>C
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ENSP00000478688.1:n.559+2020A>C
|
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NM_000488.3:c.861A>C , LRG_577t1:c.861A>C
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NP_000479.1:p.Glu287Asp
|
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XM_005245198.2:c.717A>C
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XP_005245255.1:p.Glu239Asp
|
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NM_001365052.1:c.717A>C
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NP_001351981.1:p.Glu239Asp
|
|
NM_000488.4:c.861A>C
MANE Select
|
NP_000479.1:p.Glu287Asp
|
|
NM_001365052.2:c.717A>C
|
NP_001351981.1:p.Glu239Asp
|
|
NM_001386302.1:c.984A>C
|
NP_001373231.1:p.Glu328Asp
|
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NM_001386303.1:c.942A>C
|
NP_001373232.1:p.Glu314Asp
|
|
NM_001386304.1:c.840A>C
|
NP_001373233.1:p.Glu280Asp
|
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NM_001386305.1:c.804A>C
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NP_001373234.1:p.Glu268Asp
|
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NM_001386306.1:c.645A>C
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NP_001373235.1:p.Glu215Asp
|
|