ENST00000545712.7:c.727C>A
MANE Select
|
ENSP00000445920.1:p.Pro243Thr
|
|
ENST00000537496.5:c.*292C>A
|
ENSP00000444793.1:n.*292C>A
|
|
ENST00000540016.5:c.571C>A
|
ENSP00000474582.1:p.Pro191Thr
|
|
ENST00000541763.6:c.952C>A
|
ENSP00000474981.1:n.952C>A
|
|
ENST00000544051.5:c.*608C>A
|
ENSP00000438079.1:n.*608C>A
|
|
ENST00000545712.6:c.727C>A
|
ENSP00000445920.1:p.Pro243Thr
|
|
NM_052845.3:c.727C>A
|
NP_443077.1:p.Pro243Thr
|
|
NR_038118.1:n.887C>A
|
|
|
XM_011538266.1:c.*74C>A
|
XP_011536568.1:n.*74C>A
|
|
XM_011538267.1:c.*74C>A
|
XP_011536569.1:n.*74C>A
|
|
XM_011538268.1:c.454C>A
|
XP_011536570.1:p.Pro152Thr
|
|
XM_011538269.1:c.451C>A
|
XP_011536571.1:p.Pro151Thr
|
|
XM_011538267.3:c.*74C>A
|
XP_011536569.1:n.*74C>A
|
|
XM_011538268.2:c.454C>A
|
XP_011536570.1:p.Pro152Thr
|
|
XM_011538269.2:c.451C>A
|
XP_011536571.1:p.Pro151Thr
|
|
NM_052845.4:c.727C>A
MANE Select
|
NP_443077.1:p.Pro243Thr
|
|
NR_038118.2:n.838C>A
|
|
|