ENST00000545712.7:c.646C>T
MANE Select
|
ENSP00000445920.1:p.Leu216Phe
|
|
ENST00000537496.5:c.*211C>T
|
ENSP00000444793.1:n.*211C>T
|
|
ENST00000540016.5:c.490C>T
|
ENSP00000474582.1:p.Leu164Phe
|
|
ENST00000541763.6:c.871C>T
|
ENSP00000474981.1:n.871C>T
|
|
ENST00000544051.5:c.*527C>T
|
ENSP00000438079.1:n.*527C>T
|
|
ENST00000545712.6:c.646C>T
|
ENSP00000445920.1:p.Leu216Phe
|
|
NM_052845.3:c.646C>T
|
NP_443077.1:p.Leu216Phe
|
|
NR_038118.1:n.806C>T
|
|
|
XM_011538266.1:c.491C>T
|
XP_011536568.1:p.Thr164Ile
|
|
XM_011538267.1:c.491C>T
|
XP_011536569.1:p.Thr164Ile
|
|
XM_011538268.1:c.373C>T
|
XP_011536570.1:p.Leu125Phe
|
|
XM_011538269.1:c.370C>T
|
XP_011536571.1:p.Leu124Phe
|
|
XM_011538267.3:c.491C>T
|
XP_011536569.1:p.Thr164Ile
|
|
XM_011538268.2:c.373C>T
|
XP_011536570.1:p.Leu125Phe
|
|
XM_011538269.2:c.370C>T
|
XP_011536571.1:p.Leu124Phe
|
|
NM_052845.4:c.646C>T
MANE Select
|
NP_443077.1:p.Leu216Phe
|
|
NR_038118.2:n.757C>T
|
|
|