|
NM_006767.4:c.2462T>C
MANE Select
|
NP_006758.2:p.Ile821Thr
|
|
ENST00000646124.2:c.2462T>C
MANE Select
|
ENSP00000496779.1:p.Ile821Thr
|
|
NM_006767.3:c.2462T>C
|
NP_006758.2:p.Ile821Thr
|
|
ENST00000215739.12:c.2462T>C
|
ENSP00000215739.8:p.Ile821Thr
|
|
ENST00000415817.1:c.625T>C
|
|
|
ENST00000415817.2:c.891T>C
|
|
|
ENST00000452988.5:c.624T>C
|
ENSP00000408789.1:n.624T>C
|
|
ENST00000463909.1:n.1760T>C
|
|
|
ENST00000479606.5:n.2608T>C
|
|
|
ENST00000495142.6:n.2814T>C
|
|
|
ENST00000498649.1:n.562T>C
|
|
|
ENST00000642151.1:c.2293T>C
|
|
|
ENST00000643578.1:n.2484T>C
|
|
|
ENST00000643710.1:n.1323T>C
|
|
|
ENST00000646506.1:n.2329T>C
|
|
|
ENST00000700578.1:c.2381T>C
|
ENSP00000515073.1:p.Ile794Thr
|