ENST00000673913.2:c.*144C>T
|
ENSP00000501161.2:n.*144C>T
|
|
ENST00000710286.1:c.2161C>T
|
ENSP00000518176.1:p.His721Tyr
|
|
ENST00000673903.1:c.1429C>T
|
ENSP00000501257.1:p.His477Tyr
|
|
ENST00000673913.1:c.654C>T
|
ENSP00000501161.1:n.654C>T
|
|
ENST00000302118.5:c.1804C>T
MANE Select
|
ENSP00000303208.5:p.His602Tyr
|
|
ENST00000490692.1:n.2350C>T
|
|
|
NM_174936.3:c.1804C>T , LRG_275t1:c.1804C>T
|
NP_777596.2:p.His602Tyr
|
|
NR_110451.1:n.1411C>T
|
|
|
XM_011541193.1:c.925C>T
|
XP_011539495.1:p.His309Tyr
|
|
NM_174936.4:c.1804C>T
MANE Select
|
NP_777596.2:p.His602Tyr
|
|
NR_110451.2:n.1411C>T
|
|
|