ENST00000545712.7:c.*59G>T
MANE Select
|
ENSP00000445920.1:n.*59G>T
|
|
ENST00000537496.5:c.*377G>T
|
ENSP00000444793.1:n.*377G>T
|
|
ENST00000540016.5:c.*59G>T
|
ENSP00000474582.1:n.*59G>T
|
|
ENST00000541763.6:c.1037G>T
|
ENSP00000474981.1:n.1037G>T
|
|
ENST00000544051.5:c.*693G>T
|
ENSP00000438079.1:n.*693G>T
|
|
ENST00000545712.6:c.*59G>T
|
ENSP00000445920.1:n.*59G>T
|
|
NM_052845.3:c.*59G>T
|
NP_443077.1:n.*59G>T
|
|
NR_038118.1:n.972G>T
|
|
|
XM_011538266.1:c.*159G>T
|
XP_011536568.1:n.*159G>T
|
|
XM_011538267.1:c.*159G>T
|
XP_011536569.1:n.*159G>T
|
|
XM_011538268.1:c.*59G>T
|
XP_011536570.1:n.*59G>T
|
|
XM_011538269.1:c.*59G>T
|
XP_011536571.1:n.*59G>T
|
|
XM_011538267.3:c.*159G>T
|
XP_011536569.1:n.*159G>T
|
|
XM_011538268.2:c.*59G>T
|
XP_011536570.1:n.*59G>T
|
|
XM_011538269.2:c.*59G>T
|
XP_011536571.1:n.*59G>T
|
|
NM_052845.4:c.*59G>T
MANE Select
|
NP_443077.1:n.*59G>T
|
|
NR_038118.2:n.923G>T
|
|
|