ENST00000673913.2:c.1557T>A
|
ENSP00000501161.2:p.Gly519=
|
|
ENST00000710286.1:c.1914T>A
|
ENSP00000518176.1:p.Gly638=
|
|
ENST00000673903.1:c.1182T>A
|
ENSP00000501257.1:p.Gly394=
|
|
ENST00000673913.1:c.297T>A
|
ENSP00000501161.1:p.Gly99=
|
|
ENST00000302118.5:c.1557T>A
MANE Select
|
ENSP00000303208.5:p.Gly519=
|
|
ENST00000490692.1:n.2227+892T>A
|
|
|
NM_174936.3:c.1557T>A , LRG_275t1:c.1557T>A
|
NP_777596.2:p.Gly519=
|
|
NR_110451.1:n.1164T>A
|
|
|
XM_011541193.1:c.678T>A
|
XP_011539495.1:p.Gly226=
|
|
NM_174936.4:c.1557T>A
MANE Select
|
NP_777596.2:p.Gly519=
|
|
NR_110451.2:n.1164T>A
|
|
|