ENST00000673913.2:c.*199A>T
|
ENSP00000501161.2:n.*199A>T
|
|
ENST00000710286.1:c.2216A>T
|
ENSP00000518176.1:p.Glu739Val
|
|
ENST00000673903.1:c.1484A>T
|
ENSP00000501257.1:p.Glu495Val
|
|
ENST00000673913.1:c.709A>T
|
ENSP00000501161.1:n.709A>T
|
|
ENST00000302118.5:c.1859A>T
MANE Select
|
ENSP00000303208.5:p.Glu620Val
|
|
ENST00000490692.1:n.2405A>T
|
|
|
NM_174936.3:c.1859A>T , LRG_275t1:c.1859A>T
|
NP_777596.2:p.Glu620Val
|
|
NR_110451.1:n.1466A>T
|
|
|
XM_011541193.1:c.980A>T
|
XP_011539495.1:p.Glu327Val
|
|
NM_174936.4:c.1859A>T
MANE Select
|
NP_777596.2:p.Glu620Val
|
|
NR_110451.2:n.1466A>T
|
|
|