ENST00000355832.10:c.2391C>T
MANE Select
|
ENSP00000348089.5:p.Ser797=
|
|
ENST00000681632.1:n.2469C>T
|
|
|
ENST00000681659.1:c.2232C>T
|
ENSP00000505631.1:p.Ser744=
|
|
ENST00000355832.9:c.2391C>T
|
ENSP00000348089.5:p.Ser797=
|
|
ENST00000623073.3:c.*687C>T
|
ENSP00000485650.1:n.*687C>T
|
|
ENST00000623115.3:c.501C>T
|
ENSP00000485321.1:p.Ser167=
|
|
ENST00000624341.3:c.223C>T
|
|
|
NM_000124.3:c.2391C>T
|
NP_000115.1:p.Ser797=
|
|
NM_001346440.1:c.2391C>T
|
NP_001333369.1:p.Ser797=
|
|
NM_000124.4:c.2391C>T
MANE Select
|
NP_000115.1:p.Ser797=
|
|
NM_001346440.2:c.2391C>T
|
NP_001333369.1:p.Ser797=
|
|