ENST00000578493.2:n.931C>A
|
|
|
ENST00000699291.1:c.723C>A
|
ENSP00000514272.1:n.723C>A
|
|
ENST00000699292.1:n.638C>A
|
|
|
ENST00000225275.4:c.1598C>A
MANE Select
|
ENSP00000225275.3:p.Ala533Asp
|
|
ENST00000225275.3:c.1598C>A
|
ENSP00000225275.3:p.Ala533Asp
|
|
ENST00000577220.1:c.56C>A
|
ENSP00000464668.1:p.Ala19Asp
|
|
NM_000250.1:c.1598C>A , LRG_84t1:c.1598C>A
|
NP_000241.1:p.Ala533Asp
|
|
XM_011524821.1:c.1784C>A
|
XP_011523123.1:p.Ala595Asp
|
|
XM_011524822.1:c.1313C>A
|
XP_011523124.1:p.Ala438Asp
|
|
XM_011524823.1:c.*147C>A
|
XP_011523125.1:n.*147C>A
|
|
NM_000250.2:c.1598C>A
MANE Select
|
NP_000241.1:p.Ala533Asp
|
|