ENST00000527168.6:n.776A>T
|
|
|
ENST00000529110.2:c.761A>T
|
ENSP00000435349.2:p.Glu254Val
|
|
ENST00000529957.6:n.735A>T
|
|
|
ENST00000683366.1:c.*409A>T
|
ENSP00000507283.1:n.*409A>T
|
|
ENST00000683887.1:c.725A>T
|
ENSP00000506886.1:p.Glu242Val
|
|
ENST00000684100.1:n.671A>T
|
|
|
ENST00000684126.1:n.811A>T
|
|
|
ENST00000684688.1:n.1302A>T
|
|
|
ENST00000204679.9:c.677A>T
MANE Select
|
ENSP00000204679.4:p.Glu226Val
|
|
ENST00000204679.8:c.677A>T
|
ENSP00000204679.4:p.Glu226Val
|
|
ENST00000527076.1:n.1900A>T
|
|
|
ENST00000527168.5:n.844A>T
|
|
|
ENST00000529957.5:n.776A>T
|
|
|
NM_032520.4:c.677A>T
|
NP_115909.1:p.Glu226Val
|
|
XM_017023782.1:c.725A>T
|
XP_016879271.1:p.Glu242Val
|
|
XM_017023783.1:c.317A>T
|
XP_016879272.1:p.Glu106Val
|
|
NM_032520.5:c.677A>T
MANE Select
|
NP_115909.1:p.Glu226Val
|
|