ENST00000545712.7:c.687G>C
MANE Select
|
ENSP00000445920.1:p.Met229Ile
|
|
ENST00000537496.5:c.*252G>C
|
ENSP00000444793.1:n.*252G>C
|
|
ENST00000540016.5:c.531G>C
|
ENSP00000474582.1:p.Met177Ile
|
|
ENST00000541763.6:c.912G>C
|
ENSP00000474981.1:n.912G>C
|
|
ENST00000544051.5:c.*568G>C
|
ENSP00000438079.1:n.*568G>C
|
|
ENST00000545712.6:c.687G>C
|
ENSP00000445920.1:p.Met229Ile
|
|
NM_052845.3:c.687G>C
|
NP_443077.1:p.Met229Ile
|
|
NR_038118.1:n.847G>C
|
|
|
XM_011538266.1:c.*34G>C
|
XP_011536568.1:n.*34G>C
|
|
XM_011538267.1:c.*34G>C
|
XP_011536569.1:n.*34G>C
|
|
XM_011538268.1:c.414G>C
|
XP_011536570.1:p.Met138Ile
|
|
XM_011538269.1:c.411G>C
|
XP_011536571.1:p.Met137Ile
|
|
XM_011538267.3:c.*34G>C
|
XP_011536569.1:n.*34G>C
|
|
XM_011538268.2:c.414G>C
|
XP_011536570.1:p.Met138Ile
|
|
XM_011538269.2:c.411G>C
|
XP_011536571.1:p.Met137Ile
|
|
NM_052845.4:c.687G>C
MANE Select
|
NP_443077.1:p.Met229Ile
|
|
NR_038118.2:n.798G>C
|
|
|