|
NM_006767.4:c.485G>A
MANE Select
|
NP_006758.2:p.Trp162Ter
|
|
ENST00000646124.2:c.485G>A
MANE Select
|
ENSP00000496779.1:p.Trp162Ter
|
|
NM_006767.3:c.485G>A
|
NP_006758.2:p.Trp162Ter
|
|
ENST00000215739.12:c.485G>A
|
ENSP00000215739.8:p.Trp162Ter
|
|
ENST00000414985.5:c.*51G>A
|
ENSP00000397247.1:n.*51G>A
|
|
ENST00000443265.5:c.*184G>A
|
ENSP00000406466.1:n.*184G>A
|
|
ENST00000479606.5:n.631G>A
|
|
|
ENST00000480895.1:n.181G>A
|
|
|
ENST00000642151.1:c.316G>A
|
|
|
ENST00000644435.1:c.391G>A
|
|
|
ENST00000645935.1:c.428G>A
|
ENSP00000493479.1:p.Trp143Ter
|
|
ENST00000646506.1:n.64G>A
|
|
|
ENST00000700578.1:c.485G>A
|
ENSP00000515073.1:p.Trp162Ter
|