ENST00000673913.2:c.*192C>A
|
ENSP00000501161.2:n.*192C>A
|
|
ENST00000710286.1:c.2209C>A
|
ENSP00000518176.1:p.Pro737Thr
|
|
ENST00000673903.1:c.1477C>A
|
ENSP00000501257.1:p.Pro493Thr
|
|
ENST00000673913.1:c.702C>A
|
ENSP00000501161.1:n.702C>A
|
|
ENST00000302118.5:c.1852C>A
MANE Select
|
ENSP00000303208.5:p.Pro618Thr
|
|
ENST00000490692.1:n.2398C>A
|
|
|
NM_174936.3:c.1852C>A , LRG_275t1:c.1852C>A
|
NP_777596.2:p.Pro618Thr
|
|
NR_110451.1:n.1459C>A
|
|
|
XM_011541193.1:c.973C>A
|
XP_011539495.1:p.Pro325Thr
|
|
NM_174936.4:c.1852C>A
MANE Select
|
NP_777596.2:p.Pro618Thr
|
|
NR_110451.2:n.1459C>A
|
|
|