ENST00000367698.4:c.1153G>T
MANE Select
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ENSP00000356671.3:p.Gly385Cys
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ENST00000367698.3:c.1153G>T
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ENSP00000356671.3:p.Gly385Cys
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ENST00000617423.4:c.560-2059G>T
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ENSP00000478688.1:n.560-2059G>T
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NM_000488.3:c.1153G>T , LRG_577t1:c.1153G>T
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NP_000479.1:p.Gly385Cys
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XM_005245198.2:c.1009G>T
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XP_005245255.1:p.Gly337Cys
|
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NM_001365052.1:c.1009G>T
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NP_001351981.1:p.Gly337Cys
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NM_000488.4:c.1153G>T
MANE Select
|
NP_000479.1:p.Gly385Cys
|
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NM_001365052.2:c.1009G>T
|
NP_001351981.1:p.Gly337Cys
|
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NM_001386302.1:c.1276G>T
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NP_001373231.1:p.Gly426Cys
|
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NM_001386303.1:c.1234G>T
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NP_001373232.1:p.Gly412Cys
|
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NM_001386304.1:c.1132G>T
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NP_001373233.1:p.Gly378Cys
|
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NM_001386305.1:c.1096G>T
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NP_001373234.1:p.Gly366Cys
|
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NM_001386306.1:c.937G>T
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NP_001373235.1:p.Gly313Cys
|
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