ENST00000696666.1:n.364C>G
|
|
|
ENST00000704002.1:c.275C>G
|
ENSP00000515615.1:p.Ala92Gly
|
|
ENST00000704003.1:c.*129C>G
|
ENSP00000515616.1:n.*129C>G
|
|
ENST00000348035.9:c.176C>G
MANE Select
|
ENSP00000258737.7:p.Ala59Gly
|
|
ENST00000348035.8:c.176C>G
|
ENSP00000258737.7:p.Ala59Gly
|
|
ENST00000356142.4:c.176C>G
|
ENSP00000348461.4:p.Ala59Gly
|
|
ENST00000488373.5:n.407C>G
|
|
|
ENST00000497741.5:n.192C>G
|
|
|
NM_006908.4:c.176C>G
|
NP_008839.2:p.Ala59Gly
|
|
NM_018890.3:c.176C>G
|
NP_061485.1:p.Ala59Gly
|
|
NM_006908.5:c.176C>G
MANE Select
|
NP_008839.2:p.Ala59Gly
|
|
NM_018890.4:c.176C>G
|
NP_061485.1:p.Ala59Gly
|
|