ENST00000367698.4:c.1361T=
MANE Select
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ENSP00000356671.3:p.Phe454=
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|
ENST00000367698.3:c.1361T=
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ENSP00000356671.3:p.Phe454=
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|
ENST00000617423.4:c.746T=
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ENSP00000478688.1:p.Phe249=
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NM_000488.3:c.1361T= , LRG_577t1:c.1361T=
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NP_000479.1:p.Phe454=
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XM_005245198.2:c.1217T=
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XP_005245255.1:p.Phe406=
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NM_001365052.1:c.1217T=
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NP_001351981.1:p.Phe406=
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|
NM_000488.4:c.1361T=
MANE Select
|
NP_000479.1:p.Phe454=
|
|
NM_001365052.2:c.1217T=
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NP_001351981.1:p.Phe406=
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NM_001386302.1:c.1484T=
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NP_001373231.1:p.Phe495=
|
|
NM_001386303.1:c.1442T=
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NP_001373232.1:p.Phe481=
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|
NM_001386304.1:c.1340T=
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NP_001373233.1:p.Phe447=
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NM_001386305.1:c.1304T=
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NP_001373234.1:p.Phe435=
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NM_001386306.1:c.1145T=
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NP_001373235.1:p.Phe382=
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