ENST00000673913.2:c.*228T>C
|
ENSP00000501161.2:n.*228T>C
|
|
ENST00000710286.1:c.2245T>C
|
ENSP00000518176.1:p.Trp749Arg
|
|
ENST00000673903.1:c.1513T>C
|
ENSP00000501257.1:p.Trp505Arg
|
|
ENST00000673913.1:c.738T>C
|
ENSP00000501161.1:n.738T>C
|
|
ENST00000302118.5:c.1888T>C
MANE Select
|
ENSP00000303208.5:p.Trp630Arg
|
|
ENST00000490692.1:n.2434T>C
|
|
|
NM_174936.3:c.1888T>C , LRG_275t1:c.1888T>C
|
NP_777596.2:p.Trp630Arg
|
|
NR_110451.1:n.1495T>C
|
|
|
XM_011541193.1:c.1009T>C
|
XP_011539495.1:p.Trp337Arg
|
|
NM_174936.4:c.1888T>C
MANE Select
|
NP_777596.2:p.Trp630Arg
|
|
NR_110451.2:n.1495T>C
|
|
|