ENST00000593677.2:c.1729C>A
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|
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ENST00000688602.1:c.3126C>A
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ENST00000689936.1:c.3098C>A
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|
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ENST00000692547.1:n.186C>A
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ENST00000359596.8:c.14793C>A
MANE Select
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ENSP00000352608.2:p.Ala4931=
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ENST00000355481.8:c.14778C>A
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ENSP00000347667.3:p.Ala4926=
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ENST00000359596.7:c.14793C>A
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ENSP00000352608.2:p.Ala4931=
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ENST00000360985.7:c.14775C>A
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ENSP00000354254.4:p.Ala4925=
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NM_000540.2:c.14793C>A , LRG_766t1:c.14793C>A
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NP_000531.2:p.Ala4931=
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NM_001042723.1:c.14778C>A
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NP_001036188.1:p.Ala4926=
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XM_006723317.1:c.14775C>A
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XP_006723380.1:p.Ala4925=
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XM_006723319.1:c.14760C>A
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XP_006723382.1:p.Ala4920=
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XM_011527204.1:c.14790C>A
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XP_011525506.1:p.Ala4930=
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XM_011527205.1:c.14706C>A
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XP_011525507.1:p.Ala4902=
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XM_006723317.2:c.14775C>A
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XP_006723380.1:p.Ala4925=
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XM_006723319.2:c.14760C>A
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XP_006723382.1:p.Ala4920=
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XM_011527205.2:c.14706C>A
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XP_011525507.1:p.Ala4902=
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NM_000540.3:c.14793C>A
MANE Select
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NP_000531.2:p.Ala4931=
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NM_001042723.2:c.14778C>A
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NP_001036188.1:p.Ala4926=
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