ENST00000355832.10:c.3264T=
MANE Select
|
ENSP00000348089.5:p.Ser1088=
|
|
ENST00000679552.1:n.335T=
|
|
|
ENST00000679871.1:n.410T=
|
|
|
ENST00000679974.1:n.313T=
|
|
|
ENST00000681632.1:n.4667T=
|
|
|
ENST00000681659.1:c.3105T=
|
ENSP00000505631.1:p.Ser1035=
|
|
ENST00000355832.9:c.3264T=
|
ENSP00000348089.5:p.Ser1088=
|
|
ENST00000623073.3:c.*1560T=
|
ENSP00000485650.1:n.*1560T=
|
|
ENST00000623115.3:c.1374T=
|
ENSP00000485321.1:p.Ser458=
|
|
ENST00000624341.3:c.1096T=
|
|
|
NM_000124.3:c.3264T=
|
NP_000115.1:p.Ser1088=
|
|
XR_945953.1:n.243-869A=
|
|
|
NM_001346440.1:c.3264T=
|
NP_001333369.1:p.Ser1088=
|
|
NM_000124.4:c.3264T=
MANE Select
|
NP_000115.1:p.Ser1088=
|
|
NM_001346440.2:c.3264T=
|
NP_001333369.1:p.Ser1088=
|
|