ENST00000527168.6:n.914G>A
|
|
|
ENST00000529110.2:c.899G>A
|
ENSP00000435349.2:p.Arg300Lys
|
|
ENST00000529957.6:n.873G>A
|
|
|
ENST00000683366.1:c.*547G>A
|
ENSP00000507283.1:n.*547G>A
|
|
ENST00000683887.1:c.863G>A
|
ENSP00000506886.1:p.Arg288Lys
|
|
ENST00000684100.1:n.809G>A
|
|
|
ENST00000684126.1:n.949G>A
|
|
|
ENST00000684688.1:n.1440G>A
|
|
|
ENST00000204679.9:c.815G>A
MANE Select
|
ENSP00000204679.4:p.Arg272Lys
|
|
ENST00000204679.8:c.815G>A
|
ENSP00000204679.4:p.Arg272Lys
|
|
ENST00000527076.1:n.2038G>A
|
|
|
ENST00000527168.5:n.982G>A
|
|
|
ENST00000529957.5:n.914G>A
|
|
|
NM_032520.4:c.815G>A
|
NP_115909.1:p.Arg272Lys
|
|
XM_017023782.1:c.863G>A
|
XP_016879271.1:p.Arg288Lys
|
|
XM_017023783.1:c.455G>A
|
XP_016879272.1:p.Arg152Lys
|
|
NM_032520.5:c.815G>A
MANE Select
|
NP_115909.1:p.Arg272Lys
|
|