ENST00000311907.10:c.762T>G
MANE Select
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ENSP00000308541.5:p.Ala254=
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ENST00000311907.9:c.762T>G
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ENSP00000308541.5:p.Ala254=
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ENST00000442468.1:c.732T>G
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ENSP00000387413.1:p.Ala244=
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ENST00000490274.1:n.542T>G
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ENST00000530231.5:c.762T>G
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ENSP00000433907.1:p.Ala254=
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NM_000506.3:c.762T>G
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NP_000497.1:p.Ala254=
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NM_000506.4:c.762T>G , LRG_551t1:c.762T>G
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NP_000497.1:p.Ala254=
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NM_001311257.1:c.714T>G
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NP_001298186.1:p.Ala238=
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XR_428840.2:n.806T>G
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XR_428840.4:n.797T>G
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NM_000506.5:c.762T>G
MANE Select
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NP_000497.1:p.Ala254=
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NM_001311257.2:c.714T>G
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NP_001298186.1:p.Ala238=
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