ENST00000367698.4:c.797C>T
MANE Select
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ENSP00000356671.3:p.Thr266Ile
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ENST00000367698.3:c.797C>T
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ENSP00000356671.3:p.Thr266Ile
|
|
ENST00000487183.1:n.448C>T
|
|
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ENST00000617423.4:c.559+1956C>T
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ENSP00000478688.1:n.559+1956C>T
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NM_000488.3:c.797C>T , LRG_577t1:c.797C>T
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NP_000479.1:p.Thr266Ile
|
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XM_005245198.2:c.653C>T
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XP_005245255.1:p.Thr218Ile
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NM_001365052.1:c.653C>T
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NP_001351981.1:p.Thr218Ile
|
|
NM_000488.4:c.797C>T
MANE Select
|
NP_000479.1:p.Thr266Ile
|
|
NM_001365052.2:c.653C>T
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NP_001351981.1:p.Thr218Ile
|
|
NM_001386302.1:c.920C>T
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NP_001373231.1:p.Thr307Ile
|
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NM_001386303.1:c.878C>T
|
NP_001373232.1:p.Thr293Ile
|
|
NM_001386304.1:c.776C>T
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NP_001373233.1:p.Thr259Ile
|
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NM_001386305.1:c.763-23C>T
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NP_001373234.1:n.763-23C>T
|
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NM_001386306.1:c.581C>T
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NP_001373235.1:p.Thr194Ile
|
|