ENST00000371696.7:c.656_660del
MANE Select
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ENSP00000360761.2:p.Thr219ArgfsTer?
|
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ENST00000371694.7:c.560_564del
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ENSP00000360759.3:p.Thr187ArgfsTer?
|
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ENST00000371696.6:c.656_660del
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ENSP00000360761.2:p.Thr219ArgfsTer?
|
|
ENST00000472820.1:n.584_588del
|
|
|
ENST00000538402.1:c.656_660del
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ENSP00000438919.1:p.Thr219ArgfsTer?
|
|
NM_001012727.1:c.560_564del
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NP_001012745.1:p.Thr187ArgfsTer?
|
|
NM_006412.3:c.656_660del
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NP_006403.2:p.Thr219ArgfsTer?
|
|
NM_006412.4:c.656_660del
MANE Select
|
NP_006403.2:p.Thr219ArgfsTer?
|
|
NM_001012727.2:c.560_564del
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NP_001012745.1:p.Thr187ArgfsTer?
|
|