ENST00000367698.4:c.834G=
MANE Select
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ENSP00000356671.3:p.Ser278=
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ENST00000367698.3:c.834G=
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ENSP00000356671.3:p.Ser278=
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ENST00000487183.1:n.485G=
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|
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ENST00000617423.4:c.559+1993G=
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ENSP00000478688.1:n.559+1993G=
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NM_000488.3:c.834G= , LRG_577t1:c.834G=
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NP_000479.1:p.Ser278=
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XM_005245198.2:c.690G=
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XP_005245255.1:p.Ser230=
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NM_001365052.1:c.690G=
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NP_001351981.1:p.Ser230=
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NM_000488.4:c.834G=
MANE Select
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NP_000479.1:p.Ser278=
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NM_001365052.2:c.690G=
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NP_001351981.1:p.Ser230=
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NM_001386302.1:c.957G=
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NP_001373231.1:p.Ser319=
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NM_001386303.1:c.915G=
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NP_001373232.1:p.Ser305=
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NM_001386304.1:c.813G=
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NP_001373233.1:p.Ser271=
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NM_001386305.1:c.777G=
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NP_001373234.1:p.Ser259=
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NM_001386306.1:c.618G=
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NP_001373235.1:p.Ser206=
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