ENST00000706683.1:c.728-705G=
|
ENSP00000516497.1:n.728-705G=
|
|
ENST00000321562.9:c.952G=
MANE Select
|
ENSP00000317232.4:p.Gly318=
|
|
ENST00000321562.8:c.952G=
|
ENSP00000317232.4:p.Gly318=
|
|
ENST00000455106.1:c.180G=
|
|
|
ENST00000487489.1:n.565G=
|
|
|
ENST00000489591.5:c.*362G=
|
ENSP00000466352.1:n.*362G=
|
|
NM_021939.3:c.952G= , LRG_12t1:c.952G=
|
NP_068758.3:p.Gly318=
|
|
XM_011525099.1:c.952G=
|
XP_011523401.1:p.Gly318=
|
|
XM_011525100.1:c.679G=
|
XP_011523402.1:p.Gly227=
|
|
XM_011525099.3:c.952G=
|
XP_011523401.1:p.Gly318=
|
|
XM_011525100.2:c.679G=
|
XP_011523402.1:p.Gly227=
|
|
NM_021939.4:c.952G=
MANE Select
|
NP_068758.3:p.Gly318=
|
|