|
NM_021939.4:c.1137G>A
MANE Select
|
NP_068758.3:p.Val379=
|
|
ENST00000321562.9:c.1137G>A
MANE Select
|
ENSP00000317232.4:p.Val379=
|
|
NM_021939.3:c.1137G>A , LRG_12t1:c.1137G>A
|
NP_068758.3:p.Val379=
|
|
ENST00000321562.8:c.1137G>A
|
ENSP00000317232.4:p.Val379=
|
|
ENST00000455106.1:c.548G>A
|
|
|
ENST00000489591.5:c.*921G>A
|
ENSP00000466352.1:n.*921G>A
|
|
ENST00000490938.5:n.340G>A
|
|
|
ENST00000706683.1:c.801G>A
|
ENSP00000516497.1:p.Val267=
|
|
XM_011525099.1:c.1137G>A
|
XP_011523401.1:p.Val379=
|
|
XM_011525099.3:c.1137G>A
|
XP_011523401.1:p.Val379=
|
|
XM_011525100.1:c.864G>A
|
XP_011523402.1:p.Val288=
|
|
XM_011525100.2:c.864G>A
|
XP_011523402.1:p.Val288=
|