|
NM_021939.4:c.1323G>A
MANE Select
|
NP_068758.3:p.Thr441=
|
|
ENST00000321562.9:c.1323G>A
MANE Select
|
ENSP00000317232.4:p.Thr441=
|
|
NM_021939.3:c.1323G>A , LRG_12t1:c.1323G>A
|
NP_068758.3:p.Thr441=
|
|
ENST00000321562.8:c.1323G>A
|
ENSP00000317232.4:p.Thr441=
|
|
ENST00000455106.1:c.734G>A
|
|
|
ENST00000464180.1:n.571G>A
|
|
|
ENST00000489591.5:c.*1107G>A
|
ENSP00000466352.1:n.*1107G>A
|
|
ENST00000490938.5:n.526G>A
|
|
|
ENST00000706683.1:c.987G>A
|
ENSP00000516497.1:p.Thr329=
|
|
XM_011525099.1:c.1380G>A
|
XP_011523401.1:p.Thr460=
|
|
XM_011525099.3:c.1380G>A
|
XP_011523401.1:p.Thr460=
|
|
XM_011525100.1:c.1107G>A
|
XP_011523402.1:p.Thr369=
|
|
XM_011525100.2:c.1107G>A
|
XP_011523402.1:p.Thr369=
|