|
NM_001044385.3:c.278T>A
MANE Select
|
NP_001037850.1:p.Leu93Ter
|
|
ENST00000409883.7:c.278T>A
MANE Select
|
ENSP00000386264.2:p.Leu93Ter
|
|
NM_001044385.2:c.278T>A
|
NP_001037850.1:p.Leu93Ter
|
|
NM_152388.3:c.254T>A
|
NP_689601.2:p.Leu85Ter
|
|
NM_152388.4:c.254T>A
|
NP_689601.2:p.Leu85Ter
|
|
ENST00000286196.9:c.199T>A
|
ENSP00000286196.5:p.Trp67Arg
|
|
ENST00000409444.6:c.254T>A
|
ENSP00000387203.2:p.Leu85Ter
|
|
ENST00000409883.6:c.278T>A
|
ENSP00000386264.2:p.Leu93Ter
|
|
ENST00000432684.6:c.*77T>A
|
ENSP00000413230.2:n.*77T>A
|
|
ENST00000444047.6:c.*88T>A
|
ENSP00000402681.2:n.*88T>A
|
|
ENST00000471318.6:n.168T>A
|
|
|
ENST00000489550.5:n.381T>A
|
|
|
ENST00000621467.4:c.254T>A
|
ENSP00000480508.1:p.Leu85Ter
|
|
ENST00000621467.5:c.152T>A
|
ENSP00000480508.2:p.Leu51Ter
|
|
ENST00000686475.1:n.114T>A
|
|