ENST00000270357.10:c.1596del
MANE Select
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ENSP00000270357.4:p.Val533TrpfsTer?
|
|
ENST00000270357.8:c.903del
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ENSP00000270357.3:p.Val302TrpfsTer?
|
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ENST00000437406.1:c.162del
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ENSP00000403319.1:p.Val55TrpfsTer?
|
|
ENST00000451363.5:c.237del
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ENSP00000414661.1:p.Val80TrpfsTer?
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ENST00000464550.5:n.432del
|
|
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ENST00000471657.1:n.399del
|
|
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ENST00000481757.5:n.2530del
|
|
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ENST00000486058.5:n.1709del
|
|
|
ENST00000493398.5:n.742del
|
|
|
NM_018226.4:c.1596del
|
NP_060696.4:p.Val533TrpfsTer?
|
|
XM_005247036.3:c.1563del
|
XP_005247093.1:p.Val522TrpfsTer?
|
|
NM_018226.5:c.1596del
|
NP_060696.4:p.Val533TrpfsTer?
|
|
XM_005247036.4:c.1563del
|
XP_005247093.1:p.Val522TrpfsTer?
|
|
NM_018226.6:c.1596del
MANE Select
|
NP_060696.4:p.Val533TrpfsTer?
|
|