ENST00000274576.9:c.866T>G
MANE Select
|
ENSP00000274576.5:p.Leu289Arg
|
|
ENST00000274576.8:c.866T>G
|
ENSP00000274576.4:p.Leu289Arg
|
|
ENST00000455880.2:c.866T>G
|
ENSP00000411593.2:p.Leu289Arg
|
|
ENST00000462581.6:c.*624T>G
|
ENSP00000430595.1:n.*624T>G
|
|
ENST00000471351.2:n.1149T>G
|
|
|
NM_000171.3:c.866T>G
|
NP_000162.2:p.Leu289Arg
|
|
NM_001146040.1:c.866T>G
|
NP_001139512.1:p.Leu289Arg
|
|
NM_001292000.1:c.617T>G
|
NP_001278929.1:p.Leu206Arg
|
|
XM_005268412.2:c.866T>G
|
XP_005268469.1:p.Leu289Arg
|
|
NM_000171.4:c.866T>G
MANE Select
|
NP_000162.2:p.Leu289Arg
|
|
NM_001146040.2:c.866T>G
|
NP_001139512.1:p.Leu289Arg
|
|
NM_001292000.2:c.617T>G
|
NP_001278929.1:p.Leu206Arg
|
|