ENST00000696666.1:n.298T>G
|
|
|
ENST00000704002.1:c.209T>G
|
ENSP00000515615.1:p.Phe70Cys
|
|
ENST00000704003.1:c.*63T>G
|
ENSP00000515616.1:n.*63T>G
|
|
ENST00000348035.9:c.110T>G
MANE Select
|
ENSP00000258737.7:p.Phe37Cys
|
|
ENST00000348035.8:c.110T>G
|
ENSP00000258737.7:p.Phe37Cys
|
|
ENST00000356142.4:c.110T>G
|
ENSP00000348461.4:p.Phe37Cys
|
|
ENST00000488373.5:n.341T>G
|
|
|
ENST00000497741.5:n.126T>G
|
|
|
NM_006908.4:c.110T>G
|
NP_008839.2:p.Phe37Cys
|
|
NM_018890.3:c.110T>G
|
NP_061485.1:p.Phe37Cys
|
|
NM_006908.5:c.110T>G
MANE Select
|
NP_008839.2:p.Phe37Cys
|
|
NM_018890.4:c.110T>G
|
NP_061485.1:p.Phe37Cys
|
|