ENST00000706952.1:c.3087C>G
|
ENSP00000516672.1:p.Cys1029Trp
|
|
ENST00000638521.1:c.880C>G
|
|
|
ENST00000638869.1:c.389C>G
|
|
|
ENST00000639642.1:c.218C>G
|
|
|
ENST00000640694.1:c.2928C>G
|
ENSP00000492403.1:p.Cys976Trp
|
|
ENST00000642864.1:c.2928C>G
MANE Select
|
ENSP00000495726.1:p.Cys976Trp
|
|
ENST00000674510.1:c.2928C>G
|
ENSP00000502054.1:p.Cys976Trp
|
|
ENST00000674761.1:n.1235C>G
|
|
|
ENST00000675719.1:c.2898C>G
|
ENSP00000501927.1:p.Cys966Trp
|
|
ENST00000375365.2:c.2313C>G
|
ENSP00000364514.2:p.Cys771Trp
|
|
ENST00000396435.7:c.2928C>G
|
ENSP00000379712.3:p.Cys976Trp
|
|
NM_001111125.2:c.2928C>G
|
NP_001104595.1:p.Cys976Trp
|
|
NM_015075.1:c.2313C>G
|
NP_055890.1:p.Cys771Trp
|
|
XM_006724579.2:c.3024C>G
|
XP_006724642.1:p.Cys1008Trp
|
|
XM_006724580.2:c.2313C>G
|
XP_006724643.1:p.Cys771Trp
|
|
XM_006724581.2:c.3024C>G
|
XP_006724644.1:p.Cys1008Trp
|
|
XM_006724582.2:c.3024C>G
|
XP_006724645.1:p.Cys1008Trp
|
|
XM_006724583.2:c.3024C>G
|
XP_006724646.1:p.Cys1008Trp
|
|
XM_006724584.2:c.3024C>G
|
XP_006724647.1:p.Cys1008Trp
|
|
XM_011530772.1:c.2250C>G
|
XP_011529074.1:p.Cys750Trp
|
|
XM_011530773.1:c.2217C>G
|
XP_011529075.1:p.Cys739Trp
|
|
XM_011530774.1:c.3024C>G
|
XP_011529076.1:p.Cys1008Trp
|
|
XM_011530775.1:c.3024C>G
|
XP_011529077.1:p.Cys1008Trp
|
|
XM_011530776.1:c.3024C>G
|
XP_011529078.1:p.Cys1008Trp
|
|
XM_011530777.1:c.3024C>G
|
XP_011529079.1:p.Cys1008Trp
|
|
XR_938365.1:n.3251C>G
|
|
|
XM_006724579.3:c.3024C>G
|
XP_006724642.1:p.Cys1008Trp
|
|
XM_006724580.3:c.2313C>G
|
XP_006724643.1:p.Cys771Trp
|
|
XM_006724581.4:c.3024C>G
|
XP_006724644.1:p.Cys1008Trp
|
|
XM_006724582.4:c.3024C>G
|
XP_006724645.1:p.Cys1008Trp
|
|
XM_006724583.4:c.3024C>G
|
XP_006724646.1:p.Cys1008Trp
|
|
XM_006724584.3:c.3024C>G
|
XP_006724647.1:p.Cys1008Trp
|
|
XM_011530773.2:c.2217C>G
|
XP_011529075.1:p.Cys739Trp
|
|
XM_011530774.3:c.3024C>G
|
XP_011529076.1:p.Cys1008Trp
|
|
XM_011530776.2:c.3024C>G
|
XP_011529078.1:p.Cys1008Trp
|
|
XM_011530777.2:c.3024C>G
|
XP_011529079.1:p.Cys1008Trp
|
|
XM_017029359.2:c.2898C>G
|
XP_016884848.1:p.Cys966Trp
|
|
XM_017029360.1:c.2430C>G
|
XP_016884849.1:p.Cys810Trp
|
|
XR_938365.2:n.3245C>G
|
|
|
NM_001111125.3:c.2928C>G
MANE Select
|
NP_001104595.1:p.Cys976Trp
|
|
NM_015075.2:c.2313C>G
|
NP_055890.1:p.Cys771Trp
|
|