ENST00000367698.4:c.1257T>G
MANE Select
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ENSP00000356671.3:p.Ala419=
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ENST00000367698.3:c.1257T>G
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ENSP00000356671.3:p.Ala419=
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ENST00000617423.4:c.642T>G
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ENSP00000478688.1:p.Ala214=
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NM_000488.3:c.1257T>G , LRG_577t1:c.1257T>G
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NP_000479.1:p.Ala419=
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XM_005245198.2:c.1113T>G
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XP_005245255.1:p.Ala371=
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NM_001365052.1:c.1113T>G
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NP_001351981.1:p.Ala371=
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NM_000488.4:c.1257T>G
MANE Select
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NP_000479.1:p.Ala419=
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NM_001365052.2:c.1113T>G
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NP_001351981.1:p.Ala371=
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NM_001386302.1:c.1380T>G
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NP_001373231.1:p.Ala460=
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NM_001386303.1:c.1338T>G
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NP_001373232.1:p.Ala446=
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NM_001386304.1:c.1236T>G
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NP_001373233.1:p.Ala412=
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NM_001386305.1:c.1200T>G
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NP_001373234.1:p.Ala400=
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NM_001386306.1:c.1041T>G
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NP_001373235.1:p.Ala347=
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