ENST00000673913.2:c.*173G=
|
ENSP00000501161.2:n.*173G=
|
|
ENST00000710286.1:c.2190G=
|
ENSP00000518176.1:p.Lys730=
|
|
ENST00000673903.1:c.1458G=
|
ENSP00000501257.1:p.Lys486=
|
|
ENST00000673913.1:c.683G=
|
ENSP00000501161.1:n.683G=
|
|
ENST00000302118.5:c.1833G=
MANE Select
|
ENSP00000303208.5:p.Lys611=
|
|
ENST00000490692.1:n.2379G=
|
|
|
NM_174936.3:c.1833G= , LRG_275t1:c.1833G=
|
NP_777596.2:p.Lys611=
|
|
NR_110451.1:n.1440G=
|
|
|
XM_011541193.1:c.954G=
|
XP_011539495.1:p.Lys318=
|
|
NM_174936.4:c.1833G=
MANE Select
|
NP_777596.2:p.Lys611=
|
|
NR_110451.2:n.1440G=
|
|
|