ENST00000328300.11:c.4064A>C
MANE Select
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ENSP00000331902.7:p.Glu1355Ala
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ENST00000361603.7:c.4046A>C
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ENSP00000354505.2:p.Glu1349Ala
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ENST00000510690.2:n.558A>C
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ENST00000328300.10:c.4064A>C
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ENSP00000331902.6:p.Glu1355Ala
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ENST00000361603.6:c.4046A>C
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ENSP00000354505.2:p.Glu1349Ala
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ENST00000489230.1:n.467A>C
|
|
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NM_000495.4:c.4046A>C
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NP_000486.1:p.Glu1349Ala
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NM_033380.2:c.4064A>C
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NP_203699.1:p.Glu1355Ala
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XM_005262070.2:c.4055A>C
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XP_005262127.1:p.Glu1352Ala
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XM_006724616.2:c.4064A>C
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XP_006724679.1:p.Glu1355Ala
|
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XM_011530849.1:c.3740A>C
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XP_011529151.1:p.Glu1247Ala
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XM_011530851.1:c.1637A>C
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XP_011529153.1:p.Glu546Ala
|
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XM_011530849.2:c.4079A>C
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XP_011529151.2:p.Glu1360Ala
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XM_017029259.2:c.4070A>C
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XP_016884748.1:p.Glu1357Ala
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XM_017029260.1:c.4061A>C
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XP_016884749.1:p.Glu1354Ala
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XM_017029263.2:c.2399A>C
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XP_016884752.1:p.Glu800Ala
|
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NM_000495.5:c.4046A>C
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NP_000486.1:p.Glu1349Ala
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NM_033380.3:c.4064A>C
MANE Select
|
NP_203699.1:p.Glu1355Ala
|
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