ENST00000327047.6:c.207G=
MANE Select
|
ENSP00000322280.1:p.Glu69=
|
|
ENST00000468836.2:c.183G=
|
ENSP00000419892.2:p.Glu61=
|
|
ENST00000644099.1:c.48G=
|
ENSP00000494762.1:p.Glu16=
|
|
ENST00000645441.1:c.49G=
|
|
|
ENST00000327047.5:c.207G=
|
ENSP00000322280.1:p.Glu69=
|
|
ENST00000328863.8:c.207G=
|
ENSP00000329158.4:p.Glu69=
|
|
ENST00000468836.1:c.-194G=
|
ENSP00000419892.1:n.-194G=
|
|
ENST00000472224.1:n.213G=
|
|
|
NM_001195794.1:c.207G= , LRG_700t1:c.207G=
|
NP_001182723.1:p.Glu69=
|
|
NM_001256819.1:c.207G=
|
NP_001243748.1:p.Glu69=
|
|
NM_174878.2:c.207G=
|
NP_777367.1:p.Glu69=
|
|
NR_046380.2:n.498G=
|
|
|
XR_924167.1:n.519G=
|
|
|
NM_001256819.2:c.207G=
|
NP_001243748.1:p.Glu69=
|
|
NM_174878.3:c.207G=
MANE Select
|
NP_777367.1:p.Glu69=
|
|
NR_046380.3:n.226G=
|
|
|