|
NM_006767.4:c.628C>T
MANE Select
|
NP_006758.2:p.Arg210Ter
|
|
ENST00000646124.2:c.628C>T
MANE Select
|
ENSP00000496779.1:p.Arg210Ter
|
|
NM_006767.3:c.628C>T
|
NP_006758.2:p.Arg210Ter
|
|
ENST00000215739.12:c.628C>T
|
ENSP00000215739.8:p.Arg210Ter
|
|
ENST00000414985.5:c.*194C>T
|
ENSP00000397247.1:n.*194C>T
|
|
ENST00000443265.5:c.*327C>T
|
ENSP00000406466.1:n.*327C>T
|
|
ENST00000479606.5:n.774C>T
|
|
|
ENST00000480895.1:n.324C>T
|
|
|
ENST00000497716.5:n.11C>T
|
|
|
ENST00000642151.1:c.459C>T
|
|
|
ENST00000644435.1:c.450C>T
|
|
|
ENST00000646506.1:n.207C>T
|
|
|
ENST00000700578.1:c.628C>T
|
ENSP00000515073.1:p.Arg210Ter
|