ENST00000477226.6:n.809G=
|
|
|
ENST00000683013.1:n.723G=
|
|
|
ENST00000373960.4:c.1335G=
MANE Select
|
ENSP00000363071.3:p.Thr445=
|
|
ENST00000373960.3:c.1335G=
|
ENSP00000363071.3:p.Thr445=
|
|
ENST00000483395.1:n.190G=
|
|
|
NM_001927.3:c.1335G= , LRG_380t1:c.1335G=
|
NP_001918.3:p.Thr445=
|
|
NM_001927.4:c.1335G=
MANE Select
|
NP_001918.3:p.Thr445=
|
|
NM_001382708.1:c.1332G=
|
NP_001369637.1:p.Thr444=
|
|
NM_001382709.1:c.903G=
|
NP_001369638.1:p.Thr301=
|
|
NM_001382710.1:c.1266G=
|
NP_001369639.1:p.Thr422=
|
|
NM_001382711.1:c.1314G=
|
NP_001369640.1:p.Thr438=
|
|
NM_001382712.1:c.1335G=
|
NP_001369641.1:p.Thr445=
|
|
NM_001382713.1:c.1065G=
|
NP_001369642.1:p.Thr355=
|
|