ENST00000673913.2:c.*123A>C
|
ENSP00000501161.2:n.*123A>C
|
|
ENST00000710286.1:c.2140A>C
|
ENSP00000518176.1:p.Ser714Arg
|
|
ENST00000673903.1:c.1408A>C
|
ENSP00000501257.1:p.Ser470Arg
|
|
ENST00000673913.1:c.633A>C
|
ENSP00000501161.1:n.633A>C
|
|
ENST00000302118.5:c.1783A>C
MANE Select
|
ENSP00000303208.5:p.Ser595Arg
|
|
ENST00000490692.1:n.2329A>C
|
|
|
NM_174936.3:c.1783A>C , LRG_275t1:c.1783A>C
|
NP_777596.2:p.Ser595Arg
|
|
NR_110451.1:n.1390A>C
|
|
|
XM_011541193.1:c.904A>C
|
XP_011539495.1:p.Ser302Arg
|
|
NM_174936.4:c.1783A>C
MANE Select
|
NP_777596.2:p.Ser595Arg
|
|
NR_110451.2:n.1390A>C
|
|
|