ENST00000370192.8:c.762+485G=
MANE Select
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ENSP00000359211.3:n.762+485G=
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ENST00000370192.7:c.762+485G=
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ENSP00000359211.3:n.762+485G=
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ENST00000474241.1:n.1011G=
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NM_000110.3:c.762+485G= , LRG_722t1:c.762+485G=
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NP_000101.2:n.762+485G=
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XM_005270562.3:c.762+485G=
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XP_005270619.2:n.762+485G=
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XM_006710397.2:c.762+485G=
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XP_006710460.1:n.762+485G=
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XM_006710397.3:c.762+485G=
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XP_006710460.1:n.762+485G=
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XM_017000507.1:c.651+485G=
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XP_016855996.1:n.651+485G=
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XM_017000508.2:c.267+485G=
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XP_016855997.1:n.267+485G=
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XM_017000509.2:c.267+485G=
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XP_016855998.1:n.267+485G=
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XM_017000510.1:c.267+485G=
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XP_016855999.1:n.267+485G=
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NM_000110.4:c.762+485G=
MANE Select
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NP_000101.2:n.762+485G=
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