|
NM_021939.4:c.850G>C
MANE Select
|
NP_068758.3:p.Gly284Arg
|
|
ENST00000321562.9:c.850G>C
MANE Select
|
ENSP00000317232.4:p.Gly284Arg
|
|
NM_021939.3:c.850G>C , LRG_12t1:c.850G>C
|
NP_068758.3:p.Gly284Arg
|
|
ENST00000321562.8:c.850G>C
|
ENSP00000317232.4:p.Gly284Arg
|
|
ENST00000455106.1:c.78G>C
|
|
|
ENST00000487489.1:n.463G>C
|
|
|
ENST00000489591.5:c.*260G>C
|
ENSP00000466352.1:n.*260G>C
|
|
ENST00000706683.1:c.727+805G>C
|
ENSP00000516497.1:n.727+805G>C
|
|
XM_011525099.1:c.850G>C
|
XP_011523401.1:p.Gly284Arg
|
|
XM_011525099.3:c.850G>C
|
XP_011523401.1:p.Gly284Arg
|
|
XM_011525100.1:c.577G>C
|
XP_011523402.1:p.Gly193Arg
|
|
XM_011525100.2:c.577G>C
|
XP_011523402.1:p.Gly193Arg
|