ENST00000327047.6:c.178G=
MANE Select
|
ENSP00000322280.1:p.Glu60=
|
|
ENST00000468836.2:c.154G=
|
ENSP00000419892.2:p.Glu52=
|
|
ENST00000644099.1:c.19G=
|
ENSP00000494762.1:p.Glu7=
|
|
ENST00000645441.1:c.20G=
|
|
|
ENST00000327047.5:c.178G=
|
ENSP00000322280.1:p.Glu60=
|
|
ENST00000328863.8:c.178G=
|
ENSP00000329158.4:p.Glu60=
|
|
ENST00000468836.1:c.-223G=
|
ENSP00000419892.1:n.-223G=
|
|
ENST00000472224.1:n.184G=
|
|
|
NM_001195794.1:c.178G= , LRG_700t1:c.178G=
|
NP_001182723.1:p.Glu60=
|
|
NM_001256819.1:c.178G=
|
NP_001243748.1:p.Glu60=
|
|
NM_174878.2:c.178G=
|
NP_777367.1:p.Glu60=
|
|
NR_046380.2:n.469G=
|
|
|
XR_924167.1:n.490G=
|
|
|
NM_001256819.2:c.178G=
|
NP_001243748.1:p.Glu60=
|
|
NM_174878.3:c.178G=
MANE Select
|
NP_777367.1:p.Glu60=
|
|
NR_046380.3:n.197G=
|
|
|