ENST00000545712.7:c.725A>T
MANE Select
|
ENSP00000445920.1:p.Asp242Val
|
|
ENST00000537496.5:c.*290A>T
|
ENSP00000444793.1:n.*290A>T
|
|
ENST00000540016.5:c.569A>T
|
ENSP00000474582.1:p.Asp190Val
|
|
ENST00000541763.6:c.950A>T
|
ENSP00000474981.1:n.950A>T
|
|
ENST00000544051.5:c.*606A>T
|
ENSP00000438079.1:n.*606A>T
|
|
ENST00000545712.6:c.725A>T
|
ENSP00000445920.1:p.Asp242Val
|
|
NM_052845.3:c.725A>T
|
NP_443077.1:p.Asp242Val
|
|
NR_038118.1:n.885A>T
|
|
|
XM_011538266.1:c.*72A>T
|
XP_011536568.1:n.*72A>T
|
|
XM_011538267.1:c.*72A>T
|
XP_011536569.1:n.*72A>T
|
|
XM_011538268.1:c.452A>T
|
XP_011536570.1:p.Asp151Val
|
|
XM_011538269.1:c.449A>T
|
XP_011536571.1:p.Asp150Val
|
|
XM_011538267.3:c.*72A>T
|
XP_011536569.1:n.*72A>T
|
|
XM_011538268.2:c.452A>T
|
XP_011536570.1:p.Asp151Val
|
|
XM_011538269.2:c.449A>T
|
XP_011536571.1:p.Asp150Val
|
|
NM_052845.4:c.725A>T
MANE Select
|
NP_443077.1:p.Asp242Val
|
|
NR_038118.2:n.836A>T
|
|
|