ENST00000367698.4:c.1297A>G
MANE Select
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ENSP00000356671.3:p.Thr433Ala
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ENST00000367698.3:c.1297A>G
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ENSP00000356671.3:p.Thr433Ala
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ENST00000617423.4:c.682A>G
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ENSP00000478688.1:p.Thr228Ala
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NM_000488.3:c.1297A>G , LRG_577t1:c.1297A>G
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NP_000479.1:p.Thr433Ala
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XM_005245198.2:c.1153A>G
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XP_005245255.1:p.Thr385Ala
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NM_001365052.1:c.1153A>G
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NP_001351981.1:p.Thr385Ala
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NM_000488.4:c.1297A>G
MANE Select
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NP_000479.1:p.Thr433Ala
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NM_001365052.2:c.1153A>G
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NP_001351981.1:p.Thr385Ala
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NM_001386302.1:c.1420A>G
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NP_001373231.1:p.Thr474Ala
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NM_001386303.1:c.1378A>G
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NP_001373232.1:p.Thr460Ala
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NM_001386304.1:c.1276A>G
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NP_001373233.1:p.Thr426Ala
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NM_001386305.1:c.1240A>G
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NP_001373234.1:p.Thr414Ala
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NM_001386306.1:c.1081A>G
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NP_001373235.1:p.Thr361Ala
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