ENST00000311907.10:c.714C>G
MANE Select
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ENSP00000308541.5:p.Ala238=
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ENST00000311907.9:c.714C>G
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ENSP00000308541.5:p.Ala238=
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ENST00000442468.1:c.684C>G
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ENSP00000387413.1:p.Ala228=
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ENST00000490274.1:n.494C>G
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ENST00000530231.5:c.714C>G
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ENSP00000433907.1:p.Ala238=
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NM_000506.3:c.714C>G
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NP_000497.1:p.Ala238=
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NM_000506.4:c.714C>G , LRG_551t1:c.714C>G
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NP_000497.1:p.Ala238=
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NM_001311257.1:c.666C>G
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NP_001298186.1:p.Ala222=
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XR_428840.2:n.758C>G
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XR_428840.4:n.749C>G
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NM_000506.5:c.714C>G
MANE Select
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NP_000497.1:p.Ala238=
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NM_001311257.2:c.666C>G
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NP_001298186.1:p.Ala222=
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