ENST00000673913.2:c.*349G>T
|
ENSP00000501161.2:n.*349G>T
|
|
ENST00000710286.1:c.2366G>T
|
ENSP00000518176.1:p.Gly789Val
|
|
ENST00000673903.1:c.1634G>T
|
ENSP00000501257.1:p.Gly545Val
|
|
ENST00000673913.1:c.859G>T
|
ENSP00000501161.1:n.859G>T
|
|
ENST00000302118.5:c.2009G>T
MANE Select
|
ENSP00000303208.5:p.Gly670Val
|
|
ENST00000490692.1:n.2555G>T
|
|
|
NM_174936.3:c.2009G>T , LRG_275t1:c.2009G>T
|
NP_777596.2:p.Gly670Val
|
|
NR_110451.1:n.1616G>T
|
|
|
XM_011541193.1:c.1130G>T
|
XP_011539495.1:p.Gly377Val
|
|
NM_174936.4:c.2009G>T
MANE Select
|
NP_777596.2:p.Gly670Val
|
|
NR_110451.2:n.1616G>T
|
|
|