ENST00000673913.2:c.1596C>A
|
ENSP00000501161.2:p.Ala532=
|
|
ENST00000710286.1:c.1953C>A
|
ENSP00000518176.1:p.Ala651=
|
|
ENST00000673903.1:c.1221C>A
|
ENSP00000501257.1:p.Ala407=
|
|
ENST00000673913.1:c.336C>A
|
ENSP00000501161.1:p.Ala112=
|
|
ENST00000302118.5:c.1596C>A
MANE Select
|
ENSP00000303208.5:p.Ala532=
|
|
ENST00000490692.1:n.2227+931C>A
|
|
|
NM_174936.3:c.1596C>A , LRG_275t1:c.1596C>A
|
NP_777596.2:p.Ala532=
|
|
NR_110451.1:n.1203C>A
|
|
|
XM_011541193.1:c.717C>A
|
XP_011539495.1:p.Ala239=
|
|
NM_174936.4:c.1596C>A
MANE Select
|
NP_777596.2:p.Ala532=
|
|
NR_110451.2:n.1203C>A
|
|
|