ENST00000527168.6:n.428A>T
|
|
|
ENST00000529110.2:c.413A>T
|
ENSP00000435349.2:p.Glu138Val
|
|
ENST00000529957.6:n.387A>T
|
|
|
ENST00000683366.1:c.*61A>T
|
ENSP00000507283.1:n.*61A>T
|
|
ENST00000683887.1:c.377A>T
|
ENSP00000506886.1:p.Glu126Val
|
|
ENST00000684100.1:n.323A>T
|
|
|
ENST00000684126.1:n.387A>T
|
|
|
ENST00000684688.1:n.954A>T
|
|
|
ENST00000204679.9:c.329A>T
MANE Select
|
ENSP00000204679.4:p.Glu110Val
|
|
ENST00000204679.8:c.329A>T
|
ENSP00000204679.4:p.Glu110Val
|
|
ENST00000526820.5:c.*231A>T
|
ENSP00000434413.1:n.*231A>T
|
|
ENST00000527076.1:n.1345A>T
|
|
|
ENST00000527168.5:n.365A>T
|
|
|
ENST00000529110.1:c.396A>T
|
|
|
ENST00000529957.5:n.428A>T
|
|
|
NM_032520.4:c.329A>T
|
NP_115909.1:p.Glu110Val
|
|
XM_017023782.1:c.377A>T
|
XP_016879271.1:p.Glu126Val
|
|
XM_017023783.1:c.-32A>T
|
XP_016879272.1:n.-32A>T
|
|
NM_032520.5:c.329A>T
MANE Select
|
NP_115909.1:p.Glu110Val
|
|