|
NM_006767.4:c.486G>A
MANE Select
|
NP_006758.2:p.Trp162Ter
|
|
ENST00000646124.2:c.486G>A
MANE Select
|
ENSP00000496779.1:p.Trp162Ter
|
|
NM_006767.3:c.486G>A
|
NP_006758.2:p.Trp162Ter
|
|
ENST00000215739.12:c.486G>A
|
ENSP00000215739.8:p.Trp162Ter
|
|
ENST00000414985.5:c.*52G>A
|
ENSP00000397247.1:n.*52G>A
|
|
ENST00000443265.5:c.*185G>A
|
ENSP00000406466.1:n.*185G>A
|
|
ENST00000479606.5:n.632G>A
|
|
|
ENST00000480895.1:n.182G>A
|
|
|
ENST00000642151.1:c.317G>A
|
|
|
ENST00000644435.1:c.392G>A
|
|
|
ENST00000645935.1:c.429G>A
|
ENSP00000493479.1:p.Trp143Ter
|
|
ENST00000646506.1:n.65G>A
|
|
|
ENST00000700578.1:c.486G>A
|
ENSP00000515073.1:p.Trp162Ter
|