ENST00000302850.10:c.2781C>T
MANE Select
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ENSP00000303830.4:p.Ala927=
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ENST00000302850.9:c.2781C>T
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ENSP00000303830.4:p.Ala927=
|
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ENST00000341500.9:c.2745C>T
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ENSP00000342838.4:p.Ala915=
|
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NM_000208.2:c.2781C>T
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NP_000199.2:p.Ala927=
|
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NM_000208.3:c.2781C>T
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NP_000199.2:p.Ala927=
|
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NM_001079817.1:c.2745C>T
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NP_001073285.1:p.Ala915=
|
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NM_001079817.2:c.2745C>T
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NP_001073285.1:p.Ala915=
|
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XM_011527988.1:c.2859C>T
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XP_011526290.1:p.Ala953=
|
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XM_011527989.1:c.2823C>T
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XP_011526291.1:p.Ala941=
|
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XM_011527988.2:c.2781C>T
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XP_011526290.2:p.Ala927=
|
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XM_011527989.3:c.2745C>T
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XP_011526291.2:p.Ala915=
|
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NM_000208.4:c.2781C>T
MANE Select
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NP_000199.2:p.Ala927=
|
|
NM_001079817.3:c.2745C>T
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NP_001073285.1:p.Ala915=
|
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