ENST00000545712.7:c.659T>A
MANE Select
|
ENSP00000445920.1:p.Leu220His
|
|
ENST00000537496.5:c.*224T>A
|
ENSP00000444793.1:n.*224T>A
|
|
ENST00000540016.5:c.503T>A
|
ENSP00000474582.1:p.Leu168His
|
|
ENST00000541763.6:c.884T>A
|
ENSP00000474981.1:n.884T>A
|
|
ENST00000544051.5:c.*540T>A
|
ENSP00000438079.1:n.*540T>A
|
|
ENST00000545712.6:c.659T>A
|
ENSP00000445920.1:p.Leu220His
|
|
NM_052845.3:c.659T>A
|
NP_443077.1:p.Leu220His
|
|
NR_038118.1:n.819T>A
|
|
|
XM_011538266.1:c.*6T>A
|
XP_011536568.1:n.*6T>A
|
|
XM_011538267.1:c.*6T>A
|
XP_011536569.1:n.*6T>A
|
|
XM_011538268.1:c.386T>A
|
XP_011536570.1:p.Leu129His
|
|
XM_011538269.1:c.383T>A
|
XP_011536571.1:p.Leu128His
|
|
XM_011538267.3:c.*6T>A
|
XP_011536569.1:n.*6T>A
|
|
XM_011538268.2:c.386T>A
|
XP_011536570.1:p.Leu129His
|
|
XM_011538269.2:c.383T>A
|
XP_011536571.1:p.Leu128His
|
|
NM_052845.4:c.659T>A
MANE Select
|
NP_443077.1:p.Leu220His
|
|
NR_038118.2:n.770T>A
|
|
|