ENST00000673913.2:c.*145A=
|
ENSP00000501161.2:n.*145A=
|
|
ENST00000710286.1:c.2162A=
|
ENSP00000518176.1:p.His721=
|
|
ENST00000673903.1:c.1430A=
|
ENSP00000501257.1:p.His477=
|
|
ENST00000673913.1:c.655A=
|
ENSP00000501161.1:n.655A=
|
|
ENST00000302118.5:c.1805A=
MANE Select
|
ENSP00000303208.5:p.His602=
|
|
ENST00000490692.1:n.2351A=
|
|
|
NM_174936.3:c.1805A= , LRG_275t1:c.1805A=
|
NP_777596.2:p.His602=
|
|
NR_110451.1:n.1412A=
|
|
|
XM_011541193.1:c.926A=
|
XP_011539495.1:p.His309=
|
|
NM_174936.4:c.1805A=
MANE Select
|
NP_777596.2:p.His602=
|
|
NR_110451.2:n.1412A=
|
|
|