ENST00000696666.1:n.314C>G
|
|
|
ENST00000704002.1:c.225C>G
|
ENSP00000515615.1:p.Ala75=
|
|
ENST00000704003.1:c.*79C>G
|
ENSP00000515616.1:n.*79C>G
|
|
ENST00000348035.9:c.126C>G
MANE Select
|
ENSP00000258737.7:p.Ala42=
|
|
ENST00000348035.8:c.126C>G
|
ENSP00000258737.7:p.Ala42=
|
|
ENST00000356142.4:c.126C>G
|
ENSP00000348461.4:p.Ala42=
|
|
ENST00000488373.5:n.357C>G
|
|
|
ENST00000497741.5:n.142C>G
|
|
|
NM_006908.4:c.126C>G
|
NP_008839.2:p.Ala42=
|
|
NM_018890.3:c.126C>G
|
NP_061485.1:p.Ala42=
|
|
NM_006908.5:c.126C>G
MANE Select
|
NP_008839.2:p.Ala42=
|
|
NM_018890.4:c.126C>G
|
NP_061485.1:p.Ala42=
|
|