ENST00000302850.10:c.3947A>C
MANE Select
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ENSP00000303830.4:p.Glu1316Ala
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ENST00000302850.9:c.3947A>C
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ENSP00000303830.4:p.Glu1316Ala
|
|
ENST00000341500.9:c.3911A>C
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ENSP00000342838.4:p.Glu1304Ala
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NM_000208.2:c.3947A>C
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NP_000199.2:p.Glu1316Ala
|
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NM_000208.3:c.3947A>C
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NP_000199.2:p.Glu1316Ala
|
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NM_001079817.1:c.3911A>C
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NP_001073285.1:p.Glu1304Ala
|
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NM_001079817.2:c.3911A>C
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NP_001073285.1:p.Glu1304Ala
|
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XM_011527988.1:c.4022A>C
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XP_011526290.1:p.Glu1341Ala
|
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XM_011527989.1:c.3986A>C
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XP_011526291.1:p.Glu1329Ala
|
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XM_011527988.2:c.3944A>C
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XP_011526290.2:p.Glu1315Ala
|
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XM_011527989.3:c.3908A>C
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XP_011526291.2:p.Glu1303Ala
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NM_000208.4:c.3947A>C
MANE Select
|
NP_000199.2:p.Glu1316Ala
|
|
NM_001079817.3:c.3911A>C
|
NP_001073285.1:p.Glu1304Ala
|
|