ENST00000362061.4:c.3533T>A
MANE Select
|
ENSP00000355192.3:p.Phe1178Tyr
|
|
ENST00000679417.1:c.*2696T>A
|
ENSP00000506706.1:n.*2696T>A
|
|
ENST00000680051.1:n.659T>A
|
|
|
ENST00000680059.1:c.*1051T>A
|
ENSP00000504944.1:n.*1051T>A
|
|
ENST00000681078.1:c.3533T>A
|
ENSP00000506645.1:p.Phe1178Tyr
|
|
ENST00000681190.1:c.3533T>A
|
ENSP00000506428.1:p.Phe1178Tyr
|
|
ENST00000681874.1:c.3473T>A
|
ENSP00000505162.1:p.Phe1158Tyr
|
|
ENST00000362061.3:c.3533T>A
|
ENSP00000355192.3:p.Phe1178Tyr
|
|
ENST00000367338.7:c.3533T>A
|
ENSP00000356307.3:p.Phe1178Tyr
|
|
NM_000069.2:c.3533T>A
|
NP_000060.2:p.Phe1178Tyr
|
|
XM_005245478.2:c.3533T>A
|
XP_005245535.1:p.Phe1178Tyr
|
|
XM_005245478.3:c.3533T>A
|
XP_005245535.1:p.Phe1178Tyr
|
|
NM_000069.3:c.3533T>A
MANE Select
|
NP_000060.2:p.Phe1178Tyr
|
|