ENST00000409155.8:c.879A>G
MANE Select
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ENSP00000386284.3:p.Ala293=
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ENST00000409155.7:c.879A>G
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ENSP00000386284.3:p.Ala293=
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ENST00000482847.5:n.1152A>G
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NM_000031.5:c.879A>G
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NP_000022.3:p.Ala293=
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XM_005251799.1:c.966A>G
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XP_005251856.1:p.Ala322=
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XM_011518363.1:c.1005A>G
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XP_011516665.1:p.Ala335=
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XM_011518364.1:c.906A>G
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XP_011516666.1:p.Ala302=
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NM_001003945.2:c.966A>G
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NP_001003945.1:p.Ala322=
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NM_001317745.1:c.855A>G
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NP_001304674.1:p.Ala285=
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XM_011518364.2:c.906A>G
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XP_011516666.1:p.Ala302=
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XM_024447449.1:c.966A>G
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XP_024303217.1:p.Ala322=
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NM_000031.6:c.879A>G
MANE Select
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NP_000022.3:p.Ala293=
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NM_001003945.3:c.966A>G
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NP_001003945.1:p.Ala322=
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NM_001317745.2:c.855A>G
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NP_001304674.1:p.Ala285=
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