ENST00000258494.14:c.786+308G>C
(ALDH1L2)
MANE Select
|
ENSP00000258494.9:n.786+308G>C
|
|
ENST00000547750.2:c.*31-7394C>G
(NOPCHAP1)
|
ENSP00000490830.1:n.*31-7394C>G
|
|
ENST00000652515.1:c.813+308G>C
(ALDH1L2)
|
ENSP00000499136.1:n.813+308G>C
|
|
ENST00000258494.13:c.786+308G>C
(ALDH1L2)
|
ENSP00000258494.9:n.786+308G>C
|
|
ENST00000549335.5:n.128+308G>C
(ALDH1L2)
|
|
|
ENST00000552270.1:c.*170+308G>C
(ALDH1L2)
|
ENSP00000447538.1:n.*170+308G>C
|
|
NM_001034173.3:c.786+308G>C
(ALDH1L2)
|
NP_001029345.2:n.786+308G>C
|
|
NR_027752.1:n.909+308G>C
(ALDH1L2)
|
|
|
XM_011537986.1:c.348+308G>C
(ALDH1L2)
|
XP_011536288.1:n.348+308G>C
|
|
XM_011537987.1:c.348+308G>C
(ALDH1L2)
|
XP_011536289.1:n.348+308G>C
|
|
XM_011537988.1:c.786+308G>C
(ALDH1L2)
|
XP_011536290.1:n.786+308G>C
|
|
XM_011537989.1:c.786+308G>C
(ALDH1L2)
|
XP_011536291.1:n.786+308G>C
|
|
XM_011537986.2:c.348+308G>C
(ALDH1L2)
|
XP_011536288.1:n.348+308G>C
|
|
XM_011537988.3:c.786+308G>C
(ALDH1L2)
|
XP_011536290.1:n.786+308G>C
|
|
XM_011537989.3:c.786+308G>C
(ALDH1L2)
|
XP_011536291.1:n.786+308G>C
|
|
XM_017018889.1:c.348+308G>C
(ALDH1L2)
|
XP_016874378.1:n.348+308G>C
|
|
XM_017018890.2:c.786+308G>C
(ALDH1L2)
|
XP_016874379.1:n.786+308G>C
|
|
NM_001034173.4:c.786+308G>C
(ALDH1L2)
MANE Select
|
NP_001029345.2:n.786+308G>C
|
|
NR_027752.2:n.804+308G>C
(ALDH1L2)
|
|
|