ENST00000388988.9:c.*878_*881delinsGCCT
MANE Select
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ENSP00000373640.4:n.*878_*881delinsGCCT
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ENST00000408962.6:c.662-2752_662-2749delinsGCCT
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ENSP00000386197.2:n.662-2752_662-2749delinsGCCT
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ENST00000563233.2:c.662-2752_662-2749delinsGCCT
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ENSP00000454850.1:n.662-2752_662-2749delinsGCCT
|
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ENST00000569878.5:c.2000_2003delinsGCCT
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ENSP00000455459.1:n.2000_2003delinsGCCT
|
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NM_001083612.1:c.662-2752_662-2749delinsGCCT
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NP_001077081.1:n.662-2752_662-2749delinsGCCT
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NM_001013619.3:c.*878_*881delinsGCCT
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NP_001013641.2:n.*878_*881delinsGCCT
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NM_001013619.4:c.*878_*881delinsGCCT
MANE Select
|
NP_001013641.2:n.*878_*881delinsGCCT
|
|
NM_001083612.2:c.662-2752_662-2749delinsGCCT
|
NP_001077081.1:n.662-2752_662-2749delinsGCCT
|
|