ENST00000269980.7:c.998T>G
MANE Select
|
ENSP00000269980.2:p.Ile333Ser
|
|
ENST00000269980.6:c.998T>G
|
ENSP00000269980.2:p.Ile333Ser
|
|
ENST00000457836.6:c.1007T>G
|
ENSP00000416000.2:p.Ile336Ser
|
|
ENST00000540732.3:c.1100T>G
|
ENSP00000443246.1:p.Ile367Ser
|
|
ENST00000542943.5:c.911T>G
|
ENSP00000440345.1:p.Ile304Ser
|
|
ENST00000595085.5:c.922+303T>G
|
ENSP00000471150.2:n.922+303T>G
|
|
NM_000709.3:c.998T>G
|
NP_000700.1:p.Ile333Ser
|
|
NM_001164783.1:c.995T>G
|
NP_001158255.1:p.Ile332Ser
|
|
NM_000709.4:c.998T>G
MANE Select
|
NP_000700.1:p.Ile333Ser
|
|
NM_001164783.2:c.995T>G
|
NP_001158255.1:p.Ile332Ser
|
|