|
ENST00000647720.2:c.3468+77G>T
|
ENSP00000497673.2:n.3468+77G>T
|
|
|
ENST00000647978.2:c.*3182+77G>T
|
ENSP00000497658.1:n.*3182+77G>T
|
|
|
ENST00000649781.2:c.3285+77G>T
|
ENSP00000497203.1:n.3285+77G>T
|
|
|
ENST00000685018.2:c.3468+77G>T
|
ENSP00000510194.2:n.3468+77G>T
|
|
|
ENST00000687278.2:c.3468+77G>T
|
ENSP00000509593.2:n.3468+77G>T
|
|
|
ENST00000699585.1:c.3468+77G>T
|
ENSP00000514456.1:n.3468+77G>T
|
|
|
ENST00000699598.1:c.3468+77G>T
|
ENSP00000514467.1:n.3468+77G>T
|
|
|
ENST00000699599.1:c.3468+77G>T
|
ENSP00000514468.1:n.3468+77G>T
|
|
|
ENST00000699600.1:c.3468+77G>T
|
ENSP00000514469.1:n.3468+77G>T
|
|
|
ENST00000699601.1:c.*1843+77G>T
|
ENSP00000514470.1:n.*1843+77G>T
|
|
|
ENST00000699602.1:c.3462+77G>T
|
ENSP00000514471.1:n.3462+77G>T
|
|
|
ENST00000699604.1:c.*3292+77G>T
|
ENSP00000514472.1:n.*3292+77G>T
|
|
|
ENST00000699605.1:c.3042+77G>T
|
ENSP00000514473.1:n.3042+77G>T
|
|
|
ENST00000685018.1:c.216+77G>T
|
ENSP00000510194.1:n.216+77G>T
|
|
|
ENST00000687278.1:c.1059+77G>T
|
ENSP00000509593.1:n.1059+77G>T
|
|
|
ENST00000689011.1:c.50+77G>T
|
|
|
|
ENST00000003084.11:c.3468+77G>T
MANE Select
|
ENSP00000003084.6:n.3468+77G>T
|
|
|
ENST00000647720.1:c.1118+77G>T
|
|
|
|
ENST00000648260.1:c.2250+77G>T
|
ENSP00000497957.1:n.2250+77G>T
|
|
|
ENST00000649406.1:c.3285+77G>T
|
ENSP00000497965.1:n.3285+77G>T
|
|
|
ENST00000649781.1:c.3285+77G>T
|
ENSP00000497203.1:n.3285+77G>T
|
|
|
ENST00000003084.10:c.3468+77G>T
|
ENSP00000003084.6:n.3468+77G>T
|
|
|
ENST00000426809.5:c.3378+77G>T
|
ENSP00000389119.1:n.3378+77G>T
|
|
|
ENST00000468795.1:c.293+77G>T
|
|
|
|
NM_000492.3:c.3468+77G>T , LRG_663t1:c.3468+77G>T
|
NP_000483.3:n.3468+77G>T
|
|
|
XM_011515751.1:c.3558+77G>T
|
XP_011514053.1:n.3558+77G>T
|
|
|
XM_011515752.1:c.3558+77G>T
|
XP_011514054.1:n.3558+77G>T
|
|
|
XM_011515753.1:c.3225+77G>T
|
XP_011514055.1:n.3225+77G>T
|
|
|
XM_011515754.1:c.3225+77G>T
|
XP_011514056.1:n.3225+77G>T
|
|
|
NM_000492.4:c.3468+77G>T
MANE Select
|
NP_000483.3:n.3468+77G>T
|
|
