ENST00000220616.9:c.7998A>T
MANE Select
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ENSP00000220616.4:p.Gly2666=
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ENST00000220616.8:c.7998A>T
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ENSP00000220616.4:p.Gly2666=
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ENST00000519178.5:c.3364A>T
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ENST00000519543.5:c.2397A>T
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ENSP00000430430.1:p.Gly799=
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ENST00000521107.1:c.210A>T
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ENSP00000430161.1:p.Arg70Ser
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ENST00000522691.1:n.84A>T
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ENST00000523756.5:c.4653A>T
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NM_003235.4:c.7998A>T
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NP_003226.4:p.Gly2666=
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XM_005251038.3:c.7806A>T
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XP_005251095.1:p.Gly2602=
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XM_006716622.2:c.7935A>T
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XP_006716685.1:p.Gly2645=
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XM_005251038.4:c.7806A>T
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XP_005251095.1:p.Gly2602=
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XM_006716622.3:c.7935A>T
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XP_006716685.1:p.Gly2645=
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XM_017013793.1:c.7932A>T
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XP_016869282.1:p.Gly2644=
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XM_017013794.1:c.7863A>T
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XP_016869283.1:p.Arg2621Ser
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XM_017013795.1:c.7827A>T
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XP_016869284.1:p.Gly2609=
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XM_017013796.1:c.7779A>T
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XP_016869285.1:p.Gly2593=
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XM_017013797.1:c.7737A>T
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XP_016869286.1:p.Gly2579=
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NM_003235.5:c.7998A>T
MANE Select
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NP_003226.4:p.Gly2666=
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