ENST00000053867.8:c.1297_1298delinsCG
MANE Select
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ENSP00000053867.2:p.Arg433=
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ENST00000639447.1:c.1136+380_1136+381delinsCG
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ENSP00000492014.1:n.1136+380_1136+381delinsCG
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ENST00000053867.7:c.1297_1298delinsCG
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ENSP00000053867.2:p.Arg433=
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ENST00000586443.1:c.738_739delinsCG
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ENST00000589265.5:c.826_827delinsCG
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ENSP00000467616.1:p.Arg276=
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NM_002087.3:c.1297_1298delinsCG
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NP_002078.1:p.Arg433=
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XM_005257253.1:c.1297_1298delinsCG
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XP_005257310.1:p.Arg433=
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XM_024450730.1:c.1297_1298delinsCG
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XP_024306498.1:p.Arg433=
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NM_002087.4:c.1297_1298delinsCG
MANE Select
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NP_002078.1:p.Arg433=
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