ENST00000322048.12:c.695+1G>C
MANE Select
|
ENSP00000322832.6:n.695+1G>C
|
|
ENST00000322048.11:c.695+1G>C
|
ENSP00000322832.5:n.695+1G>C
|
|
ENST00000586153.1:c.341+1G>C
|
ENSP00000464699.1:n.341+1G>C
|
|
ENST00000586336.5:n.794+1G>C
|
|
|
ENST00000586504.5:c.426-97G>C
|
|
|
ENST00000587377.5:c.*15+1G>C
|
ENSP00000468343.1:n.*15+1G>C
|
|
ENST00000587711.5:c.380+1G>C
|
ENSP00000467459.1:n.380+1G>C
|
|
ENST00000587843.5:c.*433+1G>C
|
ENSP00000465970.1:n.*433+1G>C
|
|
ENST00000588201.5:c.*686+1G>C
|
ENSP00000466529.1:n.*686+1G>C
|
|
ENST00000589543.5:n.652+1G>C
|
|
|
ENST00000591292.5:n.2024+1G>C
|
|
|
ENST00000591392.5:c.623+1G>C
|
ENSP00000467509.1:n.623+1G>C
|
|
ENST00000592019.1:c.77-122G>C
|
|
|
NM_024589.2:c.695+1G>C , LRG_455t1:c.695+1G>C
|
NP_078865.1:n.695+1G>C
|
|
NR_046480.1:n.1019+1G>C
|
|
|
XM_006720947.2:c.695+1G>C
|
XP_006721010.1:n.695+1G>C
|
|
XM_006720948.2:c.425+1G>C
|
XP_006721011.1:n.425+1G>C
|
|
XM_006720947.4:c.695+1G>C
|
XP_006721010.1:n.695+1G>C
|
|
XM_006720948.4:c.425+1G>C
|
XP_006721011.1:n.425+1G>C
|
|
NM_024589.3:c.695+1G>C
MANE Select
|
NP_078865.1:n.695+1G>C
|
|
NR_046480.2:n.702+1G>C
|
|
|