ENST00000317357.10:c.2033C>G
MANE Select
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ENSP00000318900.5:p.Ala678Gly
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ENST00000317357.9:c.2033C>G
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ENSP00000318900.5:p.Ala678Gly
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NM_018013.3:c.2033C>G
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NP_060483.3:p.Ala678Gly
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XM_005267041.3:c.2186C>G
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XP_005267098.1:p.Ala729Gly
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XM_005267042.3:c.2090C>G
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XP_005267099.1:p.Ala697Gly
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XM_011535920.1:c.2186C>G
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XP_011534222.1:p.Ala729Gly
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XM_011535921.1:c.2072C>G
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XP_011534223.1:p.Ala691Gly
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XM_011535922.1:c.1445C>G
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XP_011534224.1:p.Ala482Gly
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XM_011535923.1:c.1256C>G
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XP_011534225.1:p.Ala419Gly
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XM_005267041.4:c.2186C>G
|
XP_005267098.1:p.Ala729Gly
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XM_005267042.4:c.2090C>G
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XP_005267099.1:p.Ala697Gly
|
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XM_011535920.2:c.2186C>G
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XP_011534222.1:p.Ala729Gly
|
|
XM_011535921.2:c.2072C>G
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XP_011534223.1:p.Ala691Gly
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XM_011535923.2:c.1256C>G
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XP_011534225.1:p.Ala419Gly
|
|
XM_017010991.1:c.1586C>G
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XP_016866480.1:p.Ala529Gly
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XM_017010992.1:c.1586C>G
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XP_016866481.1:p.Ala529Gly
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XM_017010993.1:c.1586C>G
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XP_016866482.1:p.Ala529Gly
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XM_017010994.1:c.1586C>G
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XP_016866483.1:p.Ala529Gly
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NM_018013.4:c.2033C>G
MANE Select
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NP_060483.3:p.Ala678Gly
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