|
ENST00000700029.2:c.534T>C
|
ENSP00000514759.2:p.Tyr178=
|
|
|
ENST00000710265.1:c.534T>C
|
ENSP00000518161.1:p.Tyr178=
|
|
|
ENST00000472832.3:c.534T>C
|
ENSP00000483066.2:p.Tyr178=
|
|
|
ENST00000688158.2:n.1269T>C
|
|
|
|
ENST00000688922.2:c.*364T>C
|
ENSP00000508742.2:n.*364T>C
|
|
|
ENST00000700021.1:c.489T>C
|
ENSP00000514757.1:p.Tyr163=
|
|
|
ENST00000700022.1:c.493-5694T>C
|
ENSP00000514758.1:n.493-5694T>C
|
|
|
ENST00000700023.1:n.1692T>C
|
|
|
|
ENST00000700024.1:n.1926T>C
|
|
|
|
ENST00000700025.1:n.1303T>C
|
|
|
|
ENST00000700029.1:c.368T>C
|
|
|
|
ENST00000706954.1:c.534T>C
|
ENSP00000516674.1:p.Tyr178=
|
|
|
ENST00000706955.1:c.*569T>C
|
ENSP00000516675.1:n.*569T>C
|
|
|
ENST00000686459.1:c.*120T>C
|
ENSP00000508909.1:n.*120T>C
|
|
|
ENST00000688158.1:c.*645T>C
|
ENSP00000509254.1:n.*645T>C
|
|
|
ENST00000688308.1:c.534T>C
|
ENSP00000508752.1:p.Tyr178=
|
|
|
ENST00000688922.1:c.455T>C
|
|
|
|
ENST00000693560.1:c.1053T>C
|
ENSP00000509861.1:p.Tyr351=
|
|
|
ENST00000371953.8:c.534T>C
MANE Select
|
ENSP00000361021.3:p.Tyr178=
|
|
|
ENST00000371953.7:c.534T>C
|
ENSP00000361021.3:p.Tyr178=
|
|
|
NM_000314.5:c.534T>C
|
NP_000305.3:p.Tyr178=
|
|
|
NM_000314.6:c.534T>C
|
NP_000305.3:p.Tyr178=
|
|
|
NM_001304717.2:c.1053T>C
|
NP_001291646.2:p.Tyr351=
|
|
|
NM_001304718.1:c.-58T>C
|
NP_001291647.1:n.-58T>C
|
|
|
XM_006717926.2:c.489T>C
|
XP_006717989.1:p.Tyr163=
|
|
|
XM_011539981.1:c.534T>C
|
XP_011538283.1:p.Tyr178=
|
|
|
XM_011539982.1:c.438T>C
|
XP_011538284.1:p.Tyr146=
|
|
|
XR_945789.1:n.1405T>C
|
|
|
|
XR_945790.1:n.1522T>C
|
|
|
|
XR_945791.1:n.1205-5694T>C
|
|
|
|
NM_000314.7:c.534T>C
|
NP_000305.3:p.Tyr178=
|
|
|
NM_001304717.5:c.1053T>C
|
NP_001291646.4:p.Tyr351=
|
|
|
NM_001304718.2:c.-58T>C
|
NP_001291647.1:n.-58T>C
|
|
|
NM_000314.8:c.534T>C
MANE Select
|
NP_000305.3:p.Tyr178=
|
|
