|
NM_006767.4:c.272T>C
MANE Select
|
NP_006758.2:p.Met91Thr
|
|
ENST00000646124.2:c.272T>C
MANE Select
|
ENSP00000496779.1:p.Met91Thr
|
|
NM_006767.3:c.272T>C
|
NP_006758.2:p.Met91Thr
|
|
ENST00000215739.12:c.272T>C
|
ENSP00000215739.8:p.Met91Thr
|
|
ENST00000414985.5:c.272T>C
|
ENSP00000397247.1:p.Met91Thr
|
|
ENST00000443265.5:c.277T>C
|
ENSP00000406466.1:p.Cys93Arg
|
|
ENST00000479606.5:n.418T>C
|
|
|
ENST00000493460.1:n.347T>C
|
|
|
ENST00000493460.2:n.347T>C
|
|
|
ENST00000642151.1:c.183T>C
|
|
|
ENST00000644435.1:c.178T>C
|
|
|
ENST00000645935.1:c.264-1655T>C
|
ENSP00000493479.1:n.264-1655T>C
|
|
ENST00000700578.1:c.272T>C
|
ENSP00000515073.1:p.Met91Thr
|