ENST00000545712.7:c.645-326T>C
MANE Select
|
ENSP00000445920.1:n.645-326T>C
|
|
ENST00000537496.5:c.*210-326T>C
|
ENSP00000444793.1:n.*210-326T>C
|
|
ENST00000540016.5:c.489-326T>C
|
ENSP00000474582.1:n.489-326T>C
|
|
ENST00000541763.6:c.870-326T>C
|
ENSP00000474981.1:n.870-326T>C
|
|
ENST00000544051.5:c.*526-326T>C
|
ENSP00000438079.1:n.*526-326T>C
|
|
ENST00000545712.6:c.645-326T>C
|
ENSP00000445920.1:n.645-326T>C
|
|
NM_052845.3:c.645-326T>C
|
NP_443077.1:n.645-326T>C
|
|
NR_038118.1:n.805-326T>C
|
|
|
XM_011538266.1:c.490-326T>C
|
XP_011536568.1:n.490-326T>C
|
|
XM_011538267.1:c.490-326T>C
|
XP_011536569.1:n.490-326T>C
|
|
XM_011538268.1:c.372-326T>C
|
XP_011536570.1:n.372-326T>C
|
|
XM_011538269.1:c.369-326T>C
|
XP_011536571.1:n.369-326T>C
|
|
XM_011538267.3:c.490-326T>C
|
XP_011536569.1:n.490-326T>C
|
|
XM_011538268.2:c.372-326T>C
|
XP_011536570.1:n.372-326T>C
|
|
XM_011538269.2:c.369-326T>C
|
XP_011536571.1:n.369-326T>C
|
|
NM_052845.4:c.645-326T>C
MANE Select
|
NP_443077.1:n.645-326T>C
|
|
NR_038118.2:n.756-326T>C
|
|
|