ENST00000483750.6:n.794C>A
|
|
|
ENST00000490627.2:n.198C>A
|
|
|
ENST00000698625.1:c.761C>A
|
ENSP00000513844.1:p.Pro254His
|
|
ENST00000698626.1:c.761C>A
|
ENSP00000513845.1:p.Pro254His
|
|
ENST00000698635.1:c.761C>A
|
ENSP00000513850.1:p.Pro254His
|
|
ENST00000376701.5:c.761C>A
MANE Select
|
ENSP00000365891.4:p.Pro254His
|
|
ENST00000376701.4:c.761C>A
|
ENSP00000365891.4:p.Pro254His
|
|
ENST00000465982.5:n.661C>A
|
|
|
ENST00000483750.5:n.787C>A
|
|
|
ENST00000490627.1:n.181C>A
|
|
|
NM_000377.2:c.761C>A , LRG_125t1:c.761C>A
|
NP_000368.1:p.Pro254His
|
|
XM_011543977.1:c.761C>A
|
XP_011542279.1:p.Pro254His
|
|
XM_011543977.2:c.761C>A
|
XP_011542279.1:p.Pro254His
|
|
XM_017029786.1:c.761C>A
|
XP_016885275.1:p.Pro254His
|
|
NM_000377.3:c.761C>A
MANE Select
|
NP_000368.1:p.Pro254His
|
|