ENST00000317357.10:c.1703G>C
MANE Select
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ENSP00000318900.5:p.Gly568Ala
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ENST00000317357.9:c.1703G>C
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ENSP00000318900.5:p.Gly568Ala
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NM_018013.3:c.1703G>C
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NP_060483.3:p.Gly568Ala
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XM_005267041.3:c.1856G>C
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XP_005267098.1:p.Gly619Ala
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XM_005267042.3:c.1760G>C
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XP_005267099.1:p.Gly587Ala
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XM_011535920.1:c.1856G>C
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XP_011534222.1:p.Gly619Ala
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XM_011535921.1:c.1742G>C
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XP_011534223.1:p.Gly581Ala
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XM_011535922.1:c.1115G>C
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XP_011534224.1:p.Gly372Ala
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XM_011535923.1:c.926G>C
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XP_011534225.1:p.Gly309Ala
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XM_005267041.4:c.1856G>C
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XP_005267098.1:p.Gly619Ala
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XM_005267042.4:c.1760G>C
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XP_005267099.1:p.Gly587Ala
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XM_011535920.2:c.1856G>C
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XP_011534222.1:p.Gly619Ala
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XM_011535921.2:c.1742G>C
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XP_011534223.1:p.Gly581Ala
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XM_011535923.2:c.926G>C
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XP_011534225.1:p.Gly309Ala
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XM_017010991.1:c.1256G>C
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XP_016866480.1:p.Gly419Ala
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XM_017010992.1:c.1256G>C
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XP_016866481.1:p.Gly419Ala
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XM_017010993.1:c.1256G>C
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XP_016866482.1:p.Gly419Ala
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XM_017010994.1:c.1256G>C
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XP_016866483.1:p.Gly419Ala
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NM_018013.4:c.1703G>C
MANE Select
|
NP_060483.3:p.Gly568Ala
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