ENST00000673913.2:c.1672G=
|
ENSP00000501161.2:p.Val558=
|
|
ENST00000710286.1:c.2029G=
|
ENSP00000518176.1:p.Val677=
|
|
ENST00000673903.1:c.1297G=
|
ENSP00000501257.1:p.Val433=
|
|
ENST00000673913.1:c.412G=
|
ENSP00000501161.1:p.Val138=
|
|
ENST00000302118.5:c.1672G=
MANE Select
|
ENSP00000303208.5:p.Val558=
|
|
ENST00000490692.1:n.2227+1007G=
|
|
|
NM_174936.3:c.1672G= , LRG_275t1:c.1672G=
|
NP_777596.2:p.Val558=
|
|
NR_110451.1:n.1279G=
|
|
|
XM_011541193.1:c.793G=
|
XP_011539495.1:p.Val265=
|
|
NM_174936.4:c.1672G=
MANE Select
|
NP_777596.2:p.Val558=
|
|
NR_110451.2:n.1279G=
|
|
|