ENST00000703783.1:n.889G>T
|
|
|
ENST00000703785.1:n.970G>T
|
|
|
ENST00000262464.9:c.4105G>T
MANE Select
|
ENSP00000262464.4:p.Asp1369Tyr
|
|
ENST00000262464.8:c.4105G>T
|
ENSP00000262464.4:p.Asp1369Tyr
|
|
ENST00000507835.5:c.655G>T
|
ENSP00000426839.1:p.Asp219Tyr
|
|
ENST00000508053.5:c.4105G>T
|
ENSP00000424571.1:p.Asp1369Tyr
|
|
ENST00000508989.5:c.4006G>T
|
ENSP00000425596.1:p.Asp1336Tyr
|
|
ENST00000619499.4:c.4102G>T
|
ENSP00000482132.1:p.Asp1368Tyr
|
|
NM_001999.3:c.4105G>T
|
NP_001990.2:p.Asp1369Tyr
|
|
XM_017009228.2:c.3952G>T
|
XP_016864717.1:p.Asp1318Tyr
|
|
NM_001999.4:c.4105G>T
MANE Select
|
NP_001990.2:p.Asp1369Tyr
|
|