ENST00000673913.2:c.1593G>C
|
ENSP00000501161.2:p.Gln531His
|
|
ENST00000710286.1:c.1950G>C
|
ENSP00000518176.1:p.Gln650His
|
|
ENST00000673903.1:c.1218G>C
|
ENSP00000501257.1:p.Gln406His
|
|
ENST00000673913.1:c.333G>C
|
ENSP00000501161.1:p.Gln111His
|
|
ENST00000302118.5:c.1593G>C
MANE Select
|
ENSP00000303208.5:p.Gln531His
|
|
ENST00000490692.1:n.2227+928G>C
|
|
|
NM_174936.3:c.1593G>C , LRG_275t1:c.1593G>C
|
NP_777596.2:p.Gln531His
|
|
NR_110451.1:n.1200G>C
|
|
|
XM_011541193.1:c.714G>C
|
XP_011539495.1:p.Gln238His
|
|
NM_174936.4:c.1593G>C
MANE Select
|
NP_777596.2:p.Gln531His
|
|
NR_110451.2:n.1200G>C
|
|
|