ENST00000673913.2:c.*353C=
|
ENSP00000501161.2:n.*353C=
|
|
ENST00000710286.1:c.2370C=
|
ENSP00000518176.1:p.Ala790=
|
|
ENST00000673903.1:c.1638C=
|
ENSP00000501257.1:p.Ala546=
|
|
ENST00000673913.1:c.863C=
|
ENSP00000501161.1:n.863C=
|
|
ENST00000302118.5:c.2013C=
MANE Select
|
ENSP00000303208.5:p.Ala671=
|
|
ENST00000490692.1:n.2559C=
|
|
|
NM_174936.3:c.2013C= , LRG_275t1:c.2013C=
|
NP_777596.2:p.Ala671=
|
|
NR_110451.1:n.1620C=
|
|
|
XM_011541193.1:c.1134C=
|
XP_011539495.1:p.Ala378=
|
|
NM_174936.4:c.2013C=
MANE Select
|
NP_777596.2:p.Ala671=
|
|
NR_110451.2:n.1620C=
|
|
|