ENST00000527168.6:n.914G>C
|
|
|
ENST00000529110.2:c.899G>C
|
ENSP00000435349.2:p.Arg300Thr
|
|
ENST00000529957.6:n.873G>C
|
|
|
ENST00000683366.1:c.*547G>C
|
ENSP00000507283.1:n.*547G>C
|
|
ENST00000683887.1:c.863G>C
|
ENSP00000506886.1:p.Arg288Thr
|
|
ENST00000684100.1:n.809G>C
|
|
|
ENST00000684126.1:n.949G>C
|
|
|
ENST00000684688.1:n.1440G>C
|
|
|
ENST00000204679.9:c.815G>C
MANE Select
|
ENSP00000204679.4:p.Arg272Thr
|
|
ENST00000204679.8:c.815G>C
|
ENSP00000204679.4:p.Arg272Thr
|
|
ENST00000527076.1:n.2038G>C
|
|
|
ENST00000527168.5:n.982G>C
|
|
|
ENST00000529957.5:n.914G>C
|
|
|
NM_032520.4:c.815G>C
|
NP_115909.1:p.Arg272Thr
|
|
XM_017023782.1:c.863G>C
|
XP_016879271.1:p.Arg288Thr
|
|
XM_017023783.1:c.455G>C
|
XP_016879272.1:p.Arg152Thr
|
|
NM_032520.5:c.815G>C
MANE Select
|
NP_115909.1:p.Arg272Thr
|
|