ENST00000578493.2:n.811T>A
|
|
|
ENST00000699291.1:c.603T>A
|
ENSP00000514272.1:n.603T>A
|
|
ENST00000699292.1:n.518T>A
|
|
|
ENST00000225275.4:c.1478T>A
MANE Select
|
ENSP00000225275.3:p.Val493Asp
|
|
ENST00000225275.3:c.1478T>A
|
ENSP00000225275.3:p.Val493Asp
|
|
NM_000250.1:c.1478T>A , LRG_84t1:c.1478T>A
|
NP_000241.1:p.Val493Asp
|
|
XM_011524821.1:c.1664T>A
|
XP_011523123.1:p.Val555Asp
|
|
XM_011524822.1:c.1193T>A
|
XP_011523124.1:p.Val398Asp
|
|
XM_011524823.1:c.*27T>A
|
XP_011523125.1:n.*27T>A
|
|
NM_000250.2:c.1478T>A
MANE Select
|
NP_000241.1:p.Val493Asp
|
|