ENST00000367698.4:c.929A>G
MANE Select
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ENSP00000356671.3:p.Asp310Gly
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ENST00000367698.3:c.929A>G
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ENSP00000356671.3:p.Asp310Gly
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ENST00000487183.1:n.580A>G
|
|
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ENST00000617423.4:c.559+2088A>G
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ENSP00000478688.1:n.559+2088A>G
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NM_000488.3:c.929A>G , LRG_577t1:c.929A>G
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NP_000479.1:p.Asp310Gly
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XM_005245198.2:c.785A>G
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XP_005245255.1:p.Asp262Gly
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NM_001365052.1:c.785A>G
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NP_001351981.1:p.Asp262Gly
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NM_000488.4:c.929A>G
MANE Select
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NP_000479.1:p.Asp310Gly
|
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NM_001365052.2:c.785A>G
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NP_001351981.1:p.Asp262Gly
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NM_001386302.1:c.1052A>G
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NP_001373231.1:p.Asp351Gly
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NM_001386303.1:c.1010A>G
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NP_001373232.1:p.Asp337Gly
|
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NM_001386304.1:c.908A>G
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NP_001373233.1:p.Asp303Gly
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NM_001386305.1:c.872A>G
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NP_001373234.1:p.Asp291Gly
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NM_001386306.1:c.713A>G
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NP_001373235.1:p.Asp238Gly
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