ENST00000367698.4:c.1294del
MANE Select
|
ENSP00000356671.3:p.Val432Ter
|
|
ENST00000367698.3:c.1294del
|
ENSP00000356671.3:p.Val432Ter
|
|
ENST00000617423.4:c.679del
|
ENSP00000478688.1:p.Val227Ter
|
|
NM_000488.3:c.1294del , LRG_577t1:c.1294del
|
NP_000479.1:p.Val432Ter
|
|
XM_005245198.2:c.1150del
|
XP_005245255.1:p.Val384Ter
|
|
NM_001365052.1:c.1150del
|
NP_001351981.1:p.Val384Ter
|
|
NM_000488.4:c.1294del
MANE Select
|
NP_000479.1:p.Val432Ter
|
|
NM_001365052.2:c.1150del
|
NP_001351981.1:p.Val384Ter
|
|
NM_001386302.1:c.1417del
|
NP_001373231.1:p.Val473Ter
|
|
NM_001386303.1:c.1375del
|
NP_001373232.1:p.Val459Ter
|
|
NM_001386304.1:c.1273del
|
NP_001373233.1:p.Val425Ter
|
|
NM_001386305.1:c.1237del
|
NP_001373234.1:p.Val413Ter
|
|
NM_001386306.1:c.1078del
|
NP_001373235.1:p.Val360Ter
|
|