ENST00000322048.12:c.531+144G>T
MANE Select
|
ENSP00000322832.6:n.531+144G>T
|
|
ENST00000322048.11:c.531+144G>T
|
ENSP00000322832.5:n.531+144G>T
|
|
ENST00000586153.1:c.178-241G>T
|
ENSP00000464699.1:n.178-241G>T
|
|
ENST00000586336.5:n.630+144G>T
|
|
|
ENST00000586504.5:c.311+144G>T
|
|
|
ENST00000587377.5:c.544+144G>T
|
ENSP00000468343.1:n.544+144G>T
|
|
ENST00000587711.5:c.216+144G>T
|
ENSP00000467459.1:n.216+144G>T
|
|
ENST00000587843.5:c.*269+144G>T
|
ENSP00000465970.1:n.*269+144G>T
|
|
ENST00000588201.5:c.*522+144G>T
|
ENSP00000466529.1:n.*522+144G>T
|
|
ENST00000589543.5:n.488+144G>T
|
|
|
ENST00000591292.5:n.1860+144G>T
|
|
|
ENST00000591392.5:c.459+144G>T
|
ENSP00000467509.1:n.459+144G>T
|
|
ENST00000592019.1:c.77-610G>T
|
|
|
NM_024589.2:c.531+144G>T , LRG_455t1:c.531+144G>T
|
NP_078865.1:n.531+144G>T
|
|
NR_046480.1:n.855+144G>T
|
|
|
XM_006720947.2:c.531+144G>T
|
XP_006721010.1:n.531+144G>T
|
|
XM_006720948.2:c.261+144G>T
|
XP_006721011.1:n.261+144G>T
|
|
XM_006720947.4:c.531+144G>T
|
XP_006721010.1:n.531+144G>T
|
|
XM_006720948.4:c.261+144G>T
|
XP_006721011.1:n.261+144G>T
|
|
NM_024589.3:c.531+144G>T
MANE Select
|
NP_078865.1:n.531+144G>T
|
|
NR_046480.2:n.538+144G>T
|
|
|