ENST00000322048.12:c.390G>A
MANE Select
|
ENSP00000322832.6:p.Arg130=
|
|
ENST00000322048.11:c.390G>A
|
ENSP00000322832.5:p.Arg130=
|
|
ENST00000585653.1:n.522G>A
|
|
|
ENST00000586153.1:c.135G>A
|
ENSP00000464699.1:p.Arg45=
|
|
ENST00000586336.5:n.489G>A
|
|
|
ENST00000586504.5:c.170G>A
|
|
|
ENST00000587377.5:c.390G>A
|
ENSP00000468343.1:p.Arg130=
|
|
ENST00000587711.5:c.118-1061G>A
|
ENSP00000467459.1:n.118-1061G>A
|
|
ENST00000587843.5:c.*128G>A
|
ENSP00000465970.1:n.*128G>A
|
|
ENST00000588201.5:c.*247G>A
|
ENSP00000466529.1:n.*247G>A
|
|
ENST00000589543.5:n.347G>A
|
|
|
ENST00000591292.5:n.1719G>A
|
|
|
ENST00000591392.5:c.318G>A
|
ENSP00000467509.1:p.Arg106=
|
|
ENST00000592019.1:c.76+33G>A
|
|
|
NM_024589.2:c.390G>A , LRG_455t1:c.390G>A
|
NP_078865.1:p.Arg130=
|
|
NR_046480.1:n.714G>A
|
|
|
XM_006720947.2:c.390G>A
|
XP_006721010.1:p.Arg130=
|
|
XM_006720948.2:c.120G>A
|
XP_006721011.1:p.Arg40=
|
|
XM_006720947.4:c.390G>A
|
XP_006721010.1:p.Arg130=
|
|
XM_006720948.4:c.120G>A
|
XP_006721011.1:p.Arg40=
|
|
NM_024589.3:c.390G>A
MANE Select
|
NP_078865.1:p.Arg130=
|
|
NR_046480.2:n.397G>A
|
|
|