ENST00000268695.10:c.765A>T
MANE Select
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ENSP00000268695.5:p.Gly255=
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ENST00000268695.9:c.765A>T
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ENSP00000268695.5:p.Gly255=
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ENST00000562593.5:n.4174A>T
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ENST00000562931.5:n.353A>T
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ENST00000567525.5:c.446A>T
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ENSP00000454484.1:n.446A>T
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ENST00000568613.5:c.884A>T
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ENSP00000457921.1:n.884A>T
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NM_000512.4:c.765A>T
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NP_000503.1:p.Gly255=
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XM_005256301.2:c.765A>T
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XP_005256358.1:p.Gly255=
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XM_005256302.1:c.783A>T
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XP_005256359.1:p.Gly261=
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XM_011522982.1:c.783A>T
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XP_011521284.1:p.Gly261=
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XM_011522984.1:c.783A>T
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XP_011521286.1:p.Gly261=
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NM_001323543.1:c.210A>T
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NP_001310472.1:p.Gly70=
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NM_001323544.1:c.783A>T
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NP_001310473.1:p.Gly261=
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XM_005256301.3:c.765A>T
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XP_005256358.1:p.Gly255=
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XM_011522982.2:c.783A>T
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XP_011521284.1:p.Gly261=
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XM_017023111.2:c.783A>T
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XP_016878600.1:p.Gly261=
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XM_017023112.2:c.783A>T
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XP_016878601.1:p.Gly261=
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XM_017023113.1:c.210A>T
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XP_016878602.1:p.Gly70=
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NM_000512.5:c.765A>T
MANE Select
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NP_000503.1:p.Gly255=
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NM_001323543.2:c.210A>T
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NP_001310472.1:p.Gly70=
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NM_001323544.2:c.783A>T
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NP_001310473.1:p.Gly261=
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