ENST00000355832.10:c.3747T=
MANE Select
|
ENSP00000348089.5:p.Asp1249=
|
|
ENST00000679552.1:n.818T=
|
|
|
ENST00000679871.1:n.893T=
|
|
|
ENST00000679974.1:n.796T=
|
|
|
ENST00000681632.1:n.5150T=
|
|
|
ENST00000681659.1:c.3588T=
|
ENSP00000505631.1:p.Asp1196=
|
|
ENST00000355832.9:c.3747T=
|
ENSP00000348089.5:p.Asp1249=
|
|
ENST00000465653.1:n.69T=
|
|
|
ENST00000623073.3:c.*2043T=
|
ENSP00000485650.1:n.*2043T=
|
|
ENST00000623115.3:c.1857T=
|
ENSP00000485321.1:p.Asp619=
|
|
ENST00000624341.3:c.1579T=
|
|
|
NM_000124.3:c.3747T=
|
NP_000115.1:p.Asp1249=
|
|
XR_945953.1:n.243-1352A=
|
|
|
NM_001346440.1:c.3747T=
|
NP_001333369.1:p.Asp1249=
|
|
NM_000124.4:c.3747T=
MANE Select
|
NP_000115.1:p.Asp1249=
|
|
NM_001346440.2:c.3747T=
|
NP_001333369.1:p.Asp1249=
|
|