ENST00000322048.12:c.391G=
MANE Select
|
ENSP00000322832.6:p.Asp131=
|
|
ENST00000322048.11:c.391G=
|
ENSP00000322832.5:p.Asp131=
|
|
ENST00000585653.1:n.523G=
|
|
|
ENST00000586153.1:c.136G=
|
ENSP00000464699.1:p.Asp46=
|
|
ENST00000586336.5:n.490G=
|
|
|
ENST00000586504.5:c.171G=
|
|
|
ENST00000587377.5:c.391G=
|
ENSP00000468343.1:p.Asp131=
|
|
ENST00000587711.5:c.118-1060G=
|
ENSP00000467459.1:n.118-1060G=
|
|
ENST00000587843.5:c.*129G=
|
ENSP00000465970.1:n.*129G=
|
|
ENST00000588201.5:c.*248G=
|
ENSP00000466529.1:n.*248G=
|
|
ENST00000589543.5:n.348G=
|
|
|
ENST00000591292.5:n.1720G=
|
|
|
ENST00000591392.5:c.319G=
|
ENSP00000467509.1:p.Asp107=
|
|
ENST00000592019.1:c.76+34G=
|
|
|
NM_024589.2:c.391G= , LRG_455t1:c.391G=
|
NP_078865.1:p.Asp131=
|
|
NR_046480.1:n.715G=
|
|
|
XM_006720947.2:c.391G=
|
XP_006721010.1:p.Asp131=
|
|
XM_006720948.2:c.121G=
|
XP_006721011.1:p.Asp41=
|
|
XM_006720947.4:c.391G=
|
XP_006721010.1:p.Asp131=
|
|
XM_006720948.4:c.121G=
|
XP_006721011.1:p.Asp41=
|
|
NM_024589.3:c.391G=
MANE Select
|
NP_078865.1:p.Asp131=
|
|
NR_046480.2:n.398G=
|
|
|