ENST00000706952.1:c.3087C=
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ENSP00000516672.1:p.Cys1029=
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ENST00000638521.1:c.880C=
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|
|
ENST00000638869.1:c.389C=
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|
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ENST00000639642.1:c.218C=
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|
|
ENST00000640694.1:c.2928C=
|
ENSP00000492403.1:p.Cys976=
|
|
ENST00000642864.1:c.2928C=
MANE Select
|
ENSP00000495726.1:p.Cys976=
|
|
ENST00000674510.1:c.2928C=
|
ENSP00000502054.1:p.Cys976=
|
|
ENST00000674761.1:n.1235C=
|
|
|
ENST00000675719.1:c.2898C=
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ENSP00000501927.1:p.Cys966=
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|
ENST00000375365.2:c.2313C=
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ENSP00000364514.2:p.Cys771=
|
|
ENST00000396435.7:c.2928C=
|
ENSP00000379712.3:p.Cys976=
|
|
NM_001111125.2:c.2928C=
|
NP_001104595.1:p.Cys976=
|
|
NM_015075.1:c.2313C=
|
NP_055890.1:p.Cys771=
|
|
XM_006724579.2:c.3024C=
|
XP_006724642.1:p.Cys1008=
|
|
XM_006724580.2:c.2313C=
|
XP_006724643.1:p.Cys771=
|
|
XM_006724581.2:c.3024C=
|
XP_006724644.1:p.Cys1008=
|
|
XM_006724582.2:c.3024C=
|
XP_006724645.1:p.Cys1008=
|
|
XM_006724583.2:c.3024C=
|
XP_006724646.1:p.Cys1008=
|
|
XM_006724584.2:c.3024C=
|
XP_006724647.1:p.Cys1008=
|
|
XM_011530772.1:c.2250C=
|
XP_011529074.1:p.Cys750=
|
|
XM_011530773.1:c.2217C=
|
XP_011529075.1:p.Cys739=
|
|
XM_011530774.1:c.3024C=
|
XP_011529076.1:p.Cys1008=
|
|
XM_011530775.1:c.3024C=
|
XP_011529077.1:p.Cys1008=
|
|
XM_011530776.1:c.3024C=
|
XP_011529078.1:p.Cys1008=
|
|
XM_011530777.1:c.3024C=
|
XP_011529079.1:p.Cys1008=
|
|
XR_938365.1:n.3251C=
|
|
|
XM_006724579.3:c.3024C=
|
XP_006724642.1:p.Cys1008=
|
|
XM_006724580.3:c.2313C=
|
XP_006724643.1:p.Cys771=
|
|
XM_006724581.4:c.3024C=
|
XP_006724644.1:p.Cys1008=
|
|
XM_006724582.4:c.3024C=
|
XP_006724645.1:p.Cys1008=
|
|
XM_006724583.4:c.3024C=
|
XP_006724646.1:p.Cys1008=
|
|
XM_006724584.3:c.3024C=
|
XP_006724647.1:p.Cys1008=
|
|
XM_011530773.2:c.2217C=
|
XP_011529075.1:p.Cys739=
|
|
XM_011530774.3:c.3024C=
|
XP_011529076.1:p.Cys1008=
|
|
XM_011530776.2:c.3024C=
|
XP_011529078.1:p.Cys1008=
|
|
XM_011530777.2:c.3024C=
|
XP_011529079.1:p.Cys1008=
|
|
XM_017029359.2:c.2898C=
|
XP_016884848.1:p.Cys966=
|
|
XM_017029360.1:c.2430C=
|
XP_016884849.1:p.Cys810=
|
|
XR_938365.2:n.3245C=
|
|
|
NM_001111125.3:c.2928C=
MANE Select
|
NP_001104595.1:p.Cys976=
|
|
NM_015075.2:c.2313C=
|
NP_055890.1:p.Cys771=
|
|