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NM_000025.3:c.800_808delinsCTCCGCCCG
MANE Select
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NP_000016.1:p.Ala267=
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ENST00000345060.5:c.800_808delinsCTCCGCCCG
MANE Select
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ENSP00000343782.3:p.Ala267=
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NM_000025.2:c.800_808delinsCTCCGCCCG
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NP_000016.1:p.Ala267=
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ENST00000345060.4:c.800_808delinsCTCCGCCCG
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ENSP00000343782.3:p.Ala267=
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ENST00000520341.1:n.75_83delinsCTCCGCCCG
|
|
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ENST00000520341.2:n.928_936delinsCTCCGCCCG
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|
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ENST00000614635.1:c.800_808delinsCTCCGCCCG
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ENSP00000480325.1:p.Ala267=
|
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ENST00000647937.1:c.284_292delinsCTCCGCCCG
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ENSP00000497740.1:p.Ala95=
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