ENST00000370192.8:c.2058+16269G=
MANE Select
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ENSP00000359211.3:n.2058+16269G=
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ENST00000370192.7:c.2058+16269G=
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ENSP00000359211.3:n.2058+16269G=
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NM_000110.3:c.2058+16269G= , LRG_722t1:c.2058+16269G=
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NP_000101.2:n.2058+16269G=
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XM_005270562.3:c.1842+16269G=
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XP_005270619.2:n.1842+16269G=
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XM_006710397.2:c.2058+16269G=
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XP_006710460.1:n.2058+16269G=
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XR_947619.1:n.921-9706C=
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XR_947620.1:n.921-9706C=
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XR_947621.1:n.921-9706C=
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XM_006710397.3:c.2058+16269G=
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XP_006710460.1:n.2058+16269G=
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XM_017000507.1:c.1947+16269G=
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XP_016855996.1:n.1947+16269G=
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XM_017000508.2:c.1563+16269G=
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XP_016855997.1:n.1563+16269G=
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XM_017000509.2:c.1563+16269G=
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XP_016855998.1:n.1563+16269G=
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XM_017000510.1:c.1563+16269G=
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XP_016855999.1:n.1563+16269G=
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NM_000110.4:c.2058+16269G=
MANE Select
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NP_000101.2:n.2058+16269G=
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