ENST00000394975.3:c.339T>A
MANE Select
|
ENSP00000378426.2:p.Ser113=
|
|
ENST00000300851.10:c.400T>A
|
ENSP00000300851.6:p.Ser134Thr
|
|
ENST00000319788.11:c.421T>A
|
ENSP00000326135.7:p.Ser141Thr
|
|
ENST00000354895.4:c.229T>A
|
ENSP00000346969.4:p.Ser77Thr
|
|
ENST00000394971.7:c.433T>A
|
ENSP00000378422.3:p.Ser145Thr
|
|
ENST00000394975.2:c.339T>A
|
ENSP00000378426.2:p.Ser113=
|
|
ENST00000420057.2:c.301T>A
|
|
|
ENST00000472468.1:c.24T>A
|
ENSP00000458994.1:p.Ser8=
|
|
ENST00000498155.1:c.436T>A
|
ENSP00000417662.1:p.Ser146Thr
|
|
ENST00000529564.1:c.283+2025T>A
|
ENSP00000431371.1:n.283+2025T>A
|
|
ENST00000532364.1:c.173+3270T>A
|
ENSP00000460316.1:n.173+3270T>A
|
|
ENST00000533518.5:c.212T>A
|
|
|
NM_001311311.1:c.423T>A
|
NP_001298240.1:p.Ser141=
|
|
NM_024006.4:c.339T>A
|
NP_076869.1:p.Ser113=
|
|
NM_024006.5:c.339T>A
|
NP_076869.1:p.Ser113=
|
|
NM_206824.1:c.229T>A
|
NP_996560.1:p.Ser77Thr
|
|
NM_206824.2:c.229T>A
|
NP_996560.1:p.Ser77Thr
|
|
XM_011545944.1:c.339T>A
|
XP_011544246.1:p.Ser113=
|
|
XM_011545945.1:c.229T>A
|
XP_011544247.1:p.Ser77Thr
|
|
XR_950848.1:n.1127T>A
|
|
|
NM_024006.6:c.339T>A
MANE Select
|
NP_076869.1:p.Ser113=
|
|
NM_001311311.2:c.423T>A
|
NP_001298240.1:p.Ser141=
|
|
NM_206824.3:c.229T>A
|
NP_996560.1:p.Ser77Thr
|
|