ENST00000394975.3:c.284-9G>T
MANE Select
|
ENSP00000378426.2:n.284-9G>T
|
|
ENST00000300851.10:c.345-9G>T
|
ENSP00000300851.6:n.345-9G>T
|
|
ENST00000319788.11:c.366-9G>T
|
ENSP00000326135.7:n.366-9G>T
|
|
ENST00000354895.4:c.174-9G>T
|
ENSP00000346969.4:n.174-9G>T
|
|
ENST00000394971.7:c.378-9G>T
|
ENSP00000378422.3:n.378-9G>T
|
|
ENST00000394975.2:c.284-9G>T
|
ENSP00000378426.2:n.284-9G>T
|
|
ENST00000420057.2:c.246-9G>T
|
|
|
ENST00000472468.1:c.-32-9G>T
|
ENSP00000458994.1:n.-32-9G>T
|
|
ENST00000498155.1:c.381-9G>T
|
ENSP00000417662.1:n.381-9G>T
|
|
ENST00000529564.1:c.283+1961G>T
|
ENSP00000431371.1:n.283+1961G>T
|
|
ENST00000532364.1:c.173+3206G>T
|
ENSP00000460316.1:n.173+3206G>T
|
|
ENST00000533518.5:c.157-9G>T
|
|
|
NM_001311311.1:c.368-9G>T
|
NP_001298240.1:n.368-9G>T
|
|
NM_024006.4:c.284-9G>T
|
NP_076869.1:n.284-9G>T
|
|
NM_024006.5:c.284-9G>T
|
NP_076869.1:n.284-9G>T
|
|
NM_206824.1:c.174-9G>T
|
NP_996560.1:n.174-9G>T
|
|
NM_206824.2:c.174-9G>T
|
NP_996560.1:n.174-9G>T
|
|
XM_011545944.1:c.284-9G>T
|
XP_011544246.1:n.284-9G>T
|
|
XM_011545945.1:c.174-9G>T
|
XP_011544247.1:n.174-9G>T
|
|
XR_950848.1:n.1072-9G>T
|
|
|
NM_024006.6:c.284-9G>T
MANE Select
|
NP_076869.1:n.284-9G>T
|
|
NM_001311311.2:c.368-9G>T
|
NP_001298240.1:n.368-9G>T
|
|
NM_206824.3:c.174-9G>T
|
NP_996560.1:n.174-9G>T
|
|