ENST00000545712.7:c.674G>T
MANE Select
|
ENSP00000445920.1:p.Arg225Ile
|
|
ENST00000537496.5:c.*239G>T
|
ENSP00000444793.1:n.*239G>T
|
|
ENST00000540016.5:c.518G>T
|
ENSP00000474582.1:p.Arg173Ile
|
|
ENST00000541763.6:c.899G>T
|
ENSP00000474981.1:n.899G>T
|
|
ENST00000544051.5:c.*555G>T
|
ENSP00000438079.1:n.*555G>T
|
|
ENST00000545712.6:c.674G>T
|
ENSP00000445920.1:p.Arg225Ile
|
|
NM_052845.3:c.674G>T
|
NP_443077.1:p.Arg225Ile
|
|
NR_038118.1:n.834G>T
|
|
|
XM_011538266.1:c.*21G>T
|
XP_011536568.1:n.*21G>T
|
|
XM_011538267.1:c.*21G>T
|
XP_011536569.1:n.*21G>T
|
|
XM_011538268.1:c.401G>T
|
XP_011536570.1:p.Arg134Ile
|
|
XM_011538269.1:c.398G>T
|
XP_011536571.1:p.Arg133Ile
|
|
XM_011538267.3:c.*21G>T
|
XP_011536569.1:n.*21G>T
|
|
XM_011538268.2:c.401G>T
|
XP_011536570.1:p.Arg134Ile
|
|
XM_011538269.2:c.398G>T
|
XP_011536571.1:p.Arg133Ile
|
|
NM_052845.4:c.674G>T
MANE Select
|
NP_443077.1:p.Arg225Ile
|
|
NR_038118.2:n.785G>T
|
|
|