ENST00000673913.2:c.*318G=
|
ENSP00000501161.2:n.*318G=
|
|
ENST00000710286.1:c.2335G=
|
ENSP00000518176.1:p.Asp779=
|
|
ENST00000673903.1:c.1603G=
|
ENSP00000501257.1:p.Asp535=
|
|
ENST00000673913.1:c.828G=
|
ENSP00000501161.1:n.828G=
|
|
ENST00000302118.5:c.1978G=
MANE Select
|
ENSP00000303208.5:p.Asp660=
|
|
ENST00000490692.1:n.2524G=
|
|
|
NM_174936.3:c.1978G= , LRG_275t1:c.1978G=
|
NP_777596.2:p.Asp660=
|
|
NR_110451.1:n.1585G=
|
|
|
XM_011541193.1:c.1099G=
|
XP_011539495.1:p.Asp367=
|
|
NM_174936.4:c.1978G=
MANE Select
|
NP_777596.2:p.Asp660=
|
|
NR_110451.2:n.1585G=
|
|
|