ENST00000706645.1:n.1313G=
|
|
|
ENST00000281243.10:c.266G=
MANE Select
|
ENSP00000281243.5:p.Gly89=
|
|
ENST00000281243.9:c.266G=
|
ENSP00000281243.5:p.Gly89=
|
|
ENST00000428702.6:c.173G=
|
ENSP00000390944.2:p.Gly58=
|
|
ENST00000505710.1:c.193G=
|
|
|
ENST00000507439.5:c.266G=
|
ENSP00000423227.1:p.Gly89=
|
|
ENST00000508623.5:c.266G=
|
ENSP00000426377.1:p.Gly89=
|
|
ENST00000513615.5:c.266G=
|
ENSP00000422759.1:p.Gly89=
|
|
ENST00000514300.1:c.*197G=
|
ENSP00000426039.1:n.*197G=
|
|
NM_000320.2:c.266G=
|
NP_000311.2:p.Gly89=
|
|
NM_001306140.1:c.173G=
|
NP_001293069.1:p.Gly58=
|
|
XR_241677.1:n.429G=
|
|
|
NR_156494.1:n.446G=
|
|
|
NM_000320.3:c.266G=
MANE Select
|
NP_000311.2:p.Gly89=
|
|
NM_001306140.2:c.173G=
|
NP_001293069.1:p.Gly58=
|
|
NR_156494.2:n.302G=
|
|
|