ENST00000311907.10:c.712G>T
MANE Select
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ENSP00000308541.5:p.Ala238Ser
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ENST00000311907.9:c.712G>T
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ENSP00000308541.5:p.Ala238Ser
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ENST00000442468.1:c.682G>T
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ENSP00000387413.1:p.Ala228Ser
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ENST00000490274.1:n.492G>T
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ENST00000530231.5:c.712G>T
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ENSP00000433907.1:p.Ala238Ser
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NM_000506.3:c.712G>T
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NP_000497.1:p.Ala238Ser
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NM_000506.4:c.712G>T , LRG_551t1:c.712G>T
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NP_000497.1:p.Ala238Ser
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NM_001311257.1:c.664G>T
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NP_001298186.1:p.Ala222Ser
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XR_428840.2:n.756G>T
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XR_428840.4:n.747G>T
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NM_000506.5:c.712G>T
MANE Select
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NP_000497.1:p.Ala238Ser
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NM_001311257.2:c.664G>T
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NP_001298186.1:p.Ala222Ser
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