ENST00000345060.5:c.778_779insGCA
MANE Select
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ENSP00000343782.3:p.Pro260delinsArgThr
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ENST00000520341.2:n.906_907insGCA
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ENST00000647937.1:c.262_263insGCA
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ENSP00000497740.1:p.Pro88delinsArgThr
|
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ENST00000345060.4:c.778_779insGCA
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ENSP00000343782.3:p.Pro260delinsArgThr
|
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ENST00000520341.1:n.53_54insGCA
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ENST00000614635.1:c.778_779insGCA
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ENSP00000480325.1:p.Pro260delinsArgThr
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NM_000025.2:c.778_779insGCA
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NP_000016.1:p.Pro260delinsArgThr
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NM_000025.3:c.778_779insGCA
MANE Select
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NP_000016.1:p.Pro260delinsArgThr
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