ENST00000394975.3:c.386A=
MANE Select
|
ENSP00000378426.2:p.Tyr129=
|
|
ENST00000300851.10:c.447A=
|
ENSP00000300851.6:p.Leu149=
|
|
ENST00000319788.11:c.468A=
|
ENSP00000326135.7:p.Leu156=
|
|
ENST00000354895.4:c.276A=
|
ENSP00000346969.4:p.Leu92=
|
|
ENST00000394971.7:c.480A=
|
ENSP00000378422.3:p.Leu160=
|
|
ENST00000394975.2:c.386A=
|
ENSP00000378426.2:p.Tyr129=
|
|
ENST00000420057.2:c.348A=
|
|
|
ENST00000472468.1:c.71A=
|
ENSP00000458994.1:p.Tyr24=
|
|
ENST00000498155.1:c.483A=
|
ENSP00000417662.1:p.Leu161=
|
|
ENST00000529564.1:c.283+2072A=
|
ENSP00000431371.1:n.283+2072A=
|
|
ENST00000532364.1:c.173+3317A=
|
ENSP00000460316.1:n.173+3317A=
|
|
ENST00000533518.5:c.259A=
|
|
|
NM_001311311.1:c.470A=
|
NP_001298240.1:p.Tyr157=
|
|
NM_024006.4:c.386A=
|
NP_076869.1:p.Tyr129=
|
|
NM_024006.5:c.386A=
|
NP_076869.1:p.Tyr129=
|
|
NM_206824.1:c.276A=
|
NP_996560.1:p.Leu92=
|
|
NM_206824.2:c.276A=
|
NP_996560.1:p.Leu92=
|
|
XM_011545944.1:c.386A=
|
XP_011544246.1:p.Tyr129=
|
|
XM_011545945.1:c.276A=
|
XP_011544247.1:p.Leu92=
|
|
XR_950848.1:n.1174A=
|
|
|
NM_024006.6:c.386A=
MANE Select
|
NP_076869.1:p.Tyr129=
|
|
NM_001311311.2:c.470A=
|
NP_001298240.1:p.Tyr157=
|
|
NM_206824.3:c.276A=
|
NP_996560.1:p.Leu92=
|
|