ENST00000673913.2:c.1679C>G
|
ENSP00000501161.2:p.Thr560Arg
|
|
ENST00000710286.1:c.2036C>G
|
ENSP00000518176.1:p.Thr679Arg
|
|
ENST00000673903.1:c.1304C>G
|
ENSP00000501257.1:p.Thr435Arg
|
|
ENST00000673913.1:c.419C>G
|
ENSP00000501161.1:p.Thr140Arg
|
|
ENST00000302118.5:c.1679C>G
MANE Select
|
ENSP00000303208.5:p.Thr560Arg
|
|
ENST00000490692.1:n.2227+1014C>G
|
|
|
NM_174936.3:c.1679C>G , LRG_275t1:c.1679C>G
|
NP_777596.2:p.Thr560Arg
|
|
NR_110451.1:n.1286C>G
|
|
|
XM_011541193.1:c.800C>G
|
XP_011539495.1:p.Thr267Arg
|
|
NM_174936.4:c.1679C>G
MANE Select
|
NP_777596.2:p.Thr560Arg
|
|
NR_110451.2:n.1286C>G
|
|
|