ENST00000433363.7:c.389G=
MANE Select
|
ENSP00000406220.2:p.Gly130=
|
|
ENST00000293800.10:c.369-31G=
|
ENSP00000293800.6:n.369-31G=
|
|
ENST00000381074.8:c.260G=
|
ENSP00000370464.4:p.Gly87=
|
|
ENST00000433363.6:c.389G=
|
ENSP00000406220.2:p.Gly130=
|
|
ENST00000572094.1:c.*139G=
|
ENSP00000461495.1:n.*139G=
|
|
ENST00000572352.5:c.278G=
|
ENSP00000461622.1:p.Gly93=
|
|
ENST00000573648.5:c.389G=
|
ENSP00000459372.1:p.Gly130=
|
|
ENST00000574824.5:n.1522G=
|
|
|
ENST00000575230.1:c.*235G=
|
ENSP00000460903.1:n.*235G=
|
|
ENST00000576323.1:n.419G=
|
|
|
NM_001143838.2:c.389G=
|
NP_001137310.1:p.Gly130=
|
|
NM_001284509.1:c.369-31G=
|
NP_001271438.1:n.369-31G=
|
|
NM_001284510.1:c.260G=
|
NP_001271439.1:p.Gly87=
|
|
NM_177550.4:c.389G= , LRG_1020t1:c.389G=
|
NP_808218.1:p.Gly130=
|
|
XM_006721504.2:c.278G=
|
XP_006721567.1:p.Gly93=
|
|
XM_011523795.1:c.389G=
|
XP_011522097.1:p.Gly130=
|
|
XM_011523795.3:c.389G=
|
XP_011522097.1:p.Gly130=
|
|
NM_001143838.3:c.389G=
|
NP_001137310.1:p.Gly130=
|
|
NM_001284509.2:c.369-31G=
|
NP_001271438.1:n.369-31G=
|
|
NM_001284510.2:c.260G=
|
NP_001271439.1:p.Gly87=
|
|
NM_177550.5:c.389G=
MANE Select
|
NP_808218.1:p.Gly130=
|
|