ENST00000673913.2:c.*153G=
|
ENSP00000501161.2:n.*153G=
|
|
ENST00000710286.1:c.2170G=
|
ENSP00000518176.1:p.Gly724=
|
|
ENST00000673903.1:c.1438G=
|
ENSP00000501257.1:p.Gly480=
|
|
ENST00000673913.1:c.663G=
|
ENSP00000501161.1:n.663G=
|
|
ENST00000302118.5:c.1813G=
MANE Select
|
ENSP00000303208.5:p.Gly605=
|
|
ENST00000490692.1:n.2359G=
|
|
|
NM_174936.3:c.1813G= , LRG_275t1:c.1813G=
|
NP_777596.2:p.Gly605=
|
|
NR_110451.1:n.1420G=
|
|
|
XM_011541193.1:c.934G=
|
XP_011539495.1:p.Gly312=
|
|
NM_174936.4:c.1813G=
MANE Select
|
NP_777596.2:p.Gly605=
|
|
NR_110451.2:n.1420G=
|
|
|