ENST00000673913.2:c.*175A>T
|
ENSP00000501161.2:n.*175A>T
|
|
ENST00000710286.1:c.2192A>T
|
ENSP00000518176.1:p.Glu731Val
|
|
ENST00000673903.1:c.1460A>T
|
ENSP00000501257.1:p.Glu487Val
|
|
ENST00000673913.1:c.685A>T
|
ENSP00000501161.1:n.685A>T
|
|
ENST00000302118.5:c.1835A>T
MANE Select
|
ENSP00000303208.5:p.Glu612Val
|
|
ENST00000490692.1:n.2381A>T
|
|
|
NM_174936.3:c.1835A>T , LRG_275t1:c.1835A>T
|
NP_777596.2:p.Glu612Val
|
|
NR_110451.1:n.1442A>T
|
|
|
XM_011541193.1:c.956A>T
|
XP_011539495.1:p.Glu319Val
|
|
NM_174936.4:c.1835A>T
MANE Select
|
NP_777596.2:p.Glu612Val
|
|
NR_110451.2:n.1442A>T
|
|
|