ENST00000302850.10:c.3959A>C
MANE Select
|
ENSP00000303830.4:p.Glu1320Ala
|
|
ENST00000302850.9:c.3959A>C
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ENSP00000303830.4:p.Glu1320Ala
|
|
ENST00000341500.9:c.3923A>C
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ENSP00000342838.4:p.Glu1308Ala
|
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NM_000208.2:c.3959A>C
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NP_000199.2:p.Glu1320Ala
|
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NM_000208.3:c.3959A>C
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NP_000199.2:p.Glu1320Ala
|
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NM_001079817.1:c.3923A>C
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NP_001073285.1:p.Glu1308Ala
|
|
NM_001079817.2:c.3923A>C
|
NP_001073285.1:p.Glu1308Ala
|
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XM_011527988.1:c.4034A>C
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XP_011526290.1:p.Glu1345Ala
|
|
XM_011527989.1:c.3998A>C
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XP_011526291.1:p.Glu1333Ala
|
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XM_011527988.2:c.3956A>C
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XP_011526290.2:p.Glu1319Ala
|
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XM_011527989.3:c.3920A>C
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XP_011526291.2:p.Glu1307Ala
|
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NM_000208.4:c.3959A>C
MANE Select
|
NP_000199.2:p.Glu1320Ala
|
|
NM_001079817.3:c.3923A>C
|
NP_001073285.1:p.Glu1308Ala
|
|