ENST00000355832.10:c.3264T>G
MANE Select
|
ENSP00000348089.5:p.Ser1088Arg
|
|
ENST00000679552.1:n.335T>G
|
|
|
ENST00000679871.1:n.410T>G
|
|
|
ENST00000679974.1:n.313T>G
|
|
|
ENST00000681632.1:n.4667T>G
|
|
|
ENST00000681659.1:c.3105T>G
|
ENSP00000505631.1:p.Ser1035Arg
|
|
ENST00000355832.9:c.3264T>G
|
ENSP00000348089.5:p.Ser1088Arg
|
|
ENST00000623073.3:c.*1560T>G
|
ENSP00000485650.1:n.*1560T>G
|
|
ENST00000623115.3:c.1374T>G
|
ENSP00000485321.1:p.Ser458Arg
|
|
ENST00000624341.3:c.1096T>G
|
|
|
NM_000124.3:c.3264T>G
|
NP_000115.1:p.Ser1088Arg
|
|
XR_945953.1:n.243-869A>C
|
|
|
NM_001346440.1:c.3264T>G
|
NP_001333369.1:p.Ser1088Arg
|
|
NM_000124.4:c.3264T>G
MANE Select
|
NP_000115.1:p.Ser1088Arg
|
|
NM_001346440.2:c.3264T>G
|
NP_001333369.1:p.Ser1088Arg
|
|