ENST00000367698.4:c.894C>G
MANE Select
|
ENSP00000356671.3:p.Gly298=
|
|
ENST00000367698.3:c.894C>G
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ENSP00000356671.3:p.Gly298=
|
|
ENST00000487183.1:n.545C>G
|
|
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ENST00000617423.4:c.559+2053C>G
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ENSP00000478688.1:n.559+2053C>G
|
|
NM_000488.3:c.894C>G , LRG_577t1:c.894C>G
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NP_000479.1:p.Gly298=
|
|
XM_005245198.2:c.750C>G
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XP_005245255.1:p.Gly250=
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NM_001365052.1:c.750C>G
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NP_001351981.1:p.Gly250=
|
|
NM_000488.4:c.894C>G
MANE Select
|
NP_000479.1:p.Gly298=
|
|
NM_001365052.2:c.750C>G
|
NP_001351981.1:p.Gly250=
|
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NM_001386302.1:c.1017C>G
|
NP_001373231.1:p.Gly339=
|
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NM_001386303.1:c.975C>G
|
NP_001373232.1:p.Gly325=
|
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NM_001386304.1:c.873C>G
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NP_001373233.1:p.Gly291=
|
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NM_001386305.1:c.837C>G
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NP_001373234.1:p.Gly279=
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NM_001386306.1:c.678C>G
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NP_001373235.1:p.Gly226=
|
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