ENST00000673913.2:c.*180G>A
|
ENSP00000501161.2:n.*180G>A
|
|
ENST00000710286.1:c.2197G>A
|
ENSP00000518176.1:p.Gly733Arg
|
|
ENST00000673903.1:c.1465G>A
|
ENSP00000501257.1:p.Gly489Arg
|
|
ENST00000673913.1:c.690G>A
|
ENSP00000501161.1:n.690G>A
|
|
ENST00000302118.5:c.1840G>A
MANE Select
|
ENSP00000303208.5:p.Gly614Arg
|
|
ENST00000490692.1:n.2386G>A
|
|
|
NM_174936.3:c.1840G>A , LRG_275t1:c.1840G>A
|
NP_777596.2:p.Gly614Arg
|
|
NR_110451.1:n.1447G>A
|
|
|
XM_011541193.1:c.961G>A
|
XP_011539495.1:p.Gly321Arg
|
|
NM_174936.4:c.1840G>A
MANE Select
|
NP_777596.2:p.Gly614Arg
|
|
NR_110451.2:n.1447G>A
|
|
|