ENST00000635540.2:c.*202T>G
|
ENSP00000489185.1:n.*202T>G
|
|
ENST00000399799.3:c.3567T>G
MANE Select
|
ENSP00000382697.1:p.Thr1189=
|
|
ENST00000399799.2:c.3567T>G
|
ENSP00000382697.1:p.Thr1189=
|
|
ENST00000584687.1:n.277T>G
|
|
|
ENST00000635540.1:c.*202T>G
|
ENSP00000489185.1:n.*202T>G
|
|
NM_005406.2:c.3567T>G
|
NP_005397.1:p.Thr1189=
|
|
XM_011526136.1:c.3645T>G
|
XP_011524438.1:p.Thr1215=
|
|
XM_011526137.1:c.2178T>G
|
XP_011524439.1:p.Thr726=
|
|
XM_011526137.3:c.2178T>G
|
XP_011524439.1:p.Thr726=
|
|
NM_005406.3:c.3567T>G
MANE Select
|
NP_005397.1:p.Thr1189=
|
|