ENST00000302850.10:c.3189C>T
MANE Select
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ENSP00000303830.4:p.Ala1063=
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ENST00000302850.9:c.3189C>T
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ENSP00000303830.4:p.Ala1063=
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ENST00000341500.9:c.3153C>T
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ENSP00000342838.4:p.Ala1051=
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ENST00000593970.1:n.35C>T
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NM_000208.2:c.3189C>T
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NP_000199.2:p.Ala1063=
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NM_000208.3:c.3189C>T
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NP_000199.2:p.Ala1063=
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NM_001079817.1:c.3153C>T
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NP_001073285.1:p.Ala1051=
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NM_001079817.2:c.3153C>T
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NP_001073285.1:p.Ala1051=
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XM_011527988.1:c.3264C>T
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XP_011526290.1:p.Ala1088=
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XM_011527989.1:c.3228C>T
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XP_011526291.1:p.Ala1076=
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XM_011527988.2:c.3186C>T
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XP_011526290.2:p.Ala1062=
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XM_011527989.3:c.3150C>T
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XP_011526291.2:p.Ala1050=
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NM_000208.4:c.3189C>T
MANE Select
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NP_000199.2:p.Ala1063=
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NM_001079817.3:c.3153C>T
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NP_001073285.1:p.Ala1051=
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