ENST00000673913.2:c.*113C>A
|
ENSP00000501161.2:n.*113C>A
|
|
ENST00000710286.1:c.2130C>A
|
ENSP00000518176.1:p.His710Gln
|
|
ENST00000673903.1:c.1398C>A
|
ENSP00000501257.1:p.His466Gln
|
|
ENST00000673913.1:c.623C>A
|
ENSP00000501161.1:n.623C>A
|
|
ENST00000302118.5:c.1773C>A
MANE Select
|
ENSP00000303208.5:p.His591Gln
|
|
ENST00000490692.1:n.2319C>A
|
|
|
NM_174936.3:c.1773C>A , LRG_275t1:c.1773C>A
|
NP_777596.2:p.His591Gln
|
|
NR_110451.1:n.1380C>A
|
|
|
XM_011541193.1:c.894C>A
|
XP_011539495.1:p.His298Gln
|
|
NM_174936.4:c.1773C>A
MANE Select
|
NP_777596.2:p.His591Gln
|
|
NR_110451.2:n.1380C>A
|
|
|