ENST00000559511.6:c.3713A>G
|
ENSP00000453246.2:p.Tyr1238Cys
|
|
ENST00000682065.1:c.3713A>G
|
ENSP00000507025.1:p.Tyr1238Cys
|
|
ENST00000682460.1:c.*133A>G
|
ENSP00000508334.1:n.*133A>G
|
|
ENST00000682495.1:c.*205A>G
|
ENSP00000507166.1:n.*205A>G
|
|
ENST00000682669.1:c.3512A>G
|
ENSP00000507782.1:p.Tyr1171Cys
|
|
ENST00000682788.1:c.3713A>G
|
ENSP00000508089.1:p.Tyr1238Cys
|
|
ENST00000682915.1:c.3806A>G
|
ENSP00000507493.1:n.3806A>G
|
|
ENST00000683121.1:c.3713A>G
|
ENSP00000507557.1:p.Tyr1238Cys
|
|
ENST00000683186.1:c.*476A>G
|
ENSP00000507268.1:n.*476A>G
|
|
ENST00000683496.1:c.3713A>G
|
ENSP00000506968.1:p.Tyr1238Cys
|
|
ENST00000683734.1:c.3713A>G
|
ENSP00000508319.1:p.Tyr1238Cys
|
|
ENST00000683753.1:n.2759A>G
|
|
|
ENST00000683838.1:n.787A>G
|
|
|
ENST00000684038.1:c.*133A>G
|
ENSP00000507141.1:n.*133A>G
|
|
ENST00000684235.1:c.3713A>G
|
ENSP00000508295.1:p.Tyr1238Cys
|
|
ENST00000684676.1:c.3713A>G
|
ENSP00000506948.1:p.Tyr1238Cys
|
|
ENST00000261866.12:c.3713A>G
MANE Select
|
ENSP00000261866.7:p.Tyr1238Cys
|
|
ENST00000261866.11:c.3713A>G
|
ENSP00000261866.7:p.Tyr1238Cys
|
|
ENST00000427534.6:c.3713A>G
|
ENSP00000396110.2:p.Tyr1238Cys
|
|
ENST00000535302.6:c.3713A>G
|
ENSP00000445278.2:p.Tyr1238Cys
|
|
ENST00000558093.1:n.327A>G
|
|
|
ENST00000558319.5:c.3713A>G
|
ENSP00000453599.1:p.Tyr1238Cys
|
|
NM_001160227.1:c.3713A>G
|
NP_001153699.1:p.Tyr1238Cys
|
|
NM_025137.3:c.3713A>G
|
NP_079413.3:p.Tyr1238Cys
|
|
XM_005254695.3:c.3455A>G
|
XP_005254752.1:p.Tyr1152Cys
|
|
XM_006720700.1:c.3713A>G
|
XP_006720763.1:p.Tyr1238Cys
|
|
XM_006720701.2:c.3713A>G
|
XP_006720764.1:p.Tyr1238Cys
|
|
XM_011522093.1:c.3687-437A>G
|
XP_011520395.1:n.3687-437A>G
|
|
XR_931917.1:n.3744A>G
|
|
|
XM_006720701.3:c.3713A>G
|
XP_006720764.1:p.Tyr1238Cys
|
|
XM_017022634.1:c.3713A>G
|
XP_016878123.1:p.Tyr1238Cys
|
|
XM_017022635.2:c.3713A>G
|
XP_016878124.1:p.Tyr1238Cys
|
|
XM_017022636.1:c.590A>G
|
XP_016878125.1:p.Tyr197Cys
|
|
XR_001751402.1:n.3718-437A>G
|
|
|
XR_931917.2:n.3744A>G
|
|
|
NM_025137.4:c.3713A>G
MANE Select
|
NP_079413.3:p.Tyr1238Cys
|
|
NM_001160227.2:c.3713A>G
|
NP_001153699.1:p.Tyr1238Cys
|
|