ENST00000264870.8:c.319+19251C=
MANE Select
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ENSP00000264870.3:n.319+19251C=
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ENST00000264870.7:c.319+19251C=
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ENSP00000264870.3:n.319+19251C=
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ENST00000414279.5:c.319+19251C=
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ENSP00000413334.1:n.319+19251C=
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ENST00000431222.6:c.481+19251C=
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ENSP00000416295.2:n.481+19251C=
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ENST00000479211.1:n.304+19251C=
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NM_000129.3:c.319+19251C= , LRG_549t1:c.319+19251C=
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NP_000120.2:n.319+19251C=
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XM_006715010.2:c.319+19251C=
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XP_006715073.1:n.319+19251C=
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XM_011514342.1:c.481+19251C=
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XP_011512644.1:n.481+19251C=
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NM_000129.4:c.319+19251C=
MANE Select
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NP_000120.2:n.319+19251C=
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