ENST00000367698.4:c.806A>G
MANE Select
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ENSP00000356671.3:p.Glu269Gly
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ENST00000367698.3:c.806A>G
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ENSP00000356671.3:p.Glu269Gly
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ENST00000487183.1:n.457A>G
|
|
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ENST00000617423.4:c.559+1965A>G
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ENSP00000478688.1:n.559+1965A>G
|
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NM_000488.3:c.806A>G , LRG_577t1:c.806A>G
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NP_000479.1:p.Glu269Gly
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XM_005245198.2:c.662A>G
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XP_005245255.1:p.Glu221Gly
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NM_001365052.1:c.662A>G
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NP_001351981.1:p.Glu221Gly
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NM_000488.4:c.806A>G
MANE Select
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NP_000479.1:p.Glu269Gly
|
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NM_001365052.2:c.662A>G
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NP_001351981.1:p.Glu221Gly
|
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NM_001386302.1:c.929A>G
|
NP_001373231.1:p.Glu310Gly
|
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NM_001386303.1:c.887A>G
|
NP_001373232.1:p.Glu296Gly
|
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NM_001386304.1:c.785A>G
|
NP_001373233.1:p.Glu262Gly
|
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NM_001386305.1:c.763-14A>G
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NP_001373234.1:n.763-14A>G
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NM_001386306.1:c.590A>G
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NP_001373235.1:p.Glu197Gly
|
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