ENST00000673913.2:c.*108G=
|
ENSP00000501161.2:n.*108G=
|
|
ENST00000710286.1:c.2125G=
|
ENSP00000518176.1:p.Gly709=
|
|
ENST00000673903.1:c.1393G=
|
ENSP00000501257.1:p.Gly465=
|
|
ENST00000673913.1:c.618G=
|
ENSP00000501161.1:n.618G=
|
|
ENST00000302118.5:c.1768G=
MANE Select
|
ENSP00000303208.5:p.Gly590=
|
|
ENST00000490692.1:n.2314G=
|
|
|
NM_174936.3:c.1768G= , LRG_275t1:c.1768G=
|
NP_777596.2:p.Gly590=
|
|
NR_110451.1:n.1375G=
|
|
|
XM_011541193.1:c.889G=
|
XP_011539495.1:p.Gly297=
|
|
NM_174936.4:c.1768G=
MANE Select
|
NP_777596.2:p.Gly590=
|
|
NR_110451.2:n.1375G=
|
|
|