ENST00000302850.10:c.4018G>T
MANE Select
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ENSP00000303830.4:p.Ala1340Ser
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ENST00000302850.9:c.4018G>T
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ENSP00000303830.4:p.Ala1340Ser
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ENST00000341500.9:c.3982G>T
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ENSP00000342838.4:p.Ala1328Ser
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NM_000208.2:c.4018G>T
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NP_000199.2:p.Ala1340Ser
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NM_000208.3:c.4018G>T
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NP_000199.2:p.Ala1340Ser
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NM_001079817.1:c.3982G>T
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NP_001073285.1:p.Ala1328Ser
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NM_001079817.2:c.3982G>T
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NP_001073285.1:p.Ala1328Ser
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XM_011527988.1:c.4093G>T
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XP_011526290.1:p.Ala1365Ser
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XM_011527989.1:c.4057G>T
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XP_011526291.1:p.Ala1353Ser
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XM_011527988.2:c.4015G>T
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XP_011526290.2:p.Ala1339Ser
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XM_011527989.3:c.3979G>T
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XP_011526291.2:p.Ala1327Ser
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NM_000208.4:c.4018G>T
MANE Select
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NP_000199.2:p.Ala1340Ser
|
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NM_001079817.3:c.3982G>T
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NP_001073285.1:p.Ala1328Ser
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