ENST00000700578.1:c.2073C>G
|
ENSP00000515073.1:p.Tyr691Ter
|
|
ENST00000415817.2:c.502C>G
|
|
|
ENST00000495142.6:n.2425C>G
|
|
|
ENST00000642151.1:c.1904C>G
|
|
|
ENST00000643578.1:n.2095C>G
|
|
|
ENST00000643710.1:n.934C>G
|
|
|
ENST00000646124.2:c.2073C>G
MANE Select
|
ENSP00000496779.1:p.Tyr691Ter
|
|
ENST00000646506.1:n.1940C>G
|
|
|
ENST00000215739.12:c.2073C>G
|
ENSP00000215739.8:p.Tyr691Ter
|
|
ENST00000415354.6:c.502C>G
|
ENSP00000393765.2:n.502C>G
|
|
ENST00000439171.5:c.472C>G
|
|
|
ENST00000452988.5:c.235C>G
|
ENSP00000408789.1:n.235C>G
|
|
ENST00000463909.1:n.788C>G
|
|
|
ENST00000479606.5:n.2219C>G
|
|
|
ENST00000491432.5:n.494C>G
|
|
|
ENST00000495142.5:n.689C>G
|
|
|
ENST00000498649.1:n.89C>G
|
|
|
NM_006767.3:c.2073C>G
|
NP_006758.2:p.Tyr691Ter
|
|
NM_006767.4:c.2073C>G
MANE Select
|
NP_006758.2:p.Tyr691Ter
|
|