ENST00000269980.7:c.828T>G
MANE Select
|
ENSP00000269980.2:p.Ser276=
|
|
ENST00000269980.6:c.828T>G
|
ENSP00000269980.2:p.Ser276=
|
|
ENST00000457836.6:c.762T>G
|
ENSP00000416000.2:p.Ser254=
|
|
ENST00000535632.5:n.457T>G
|
|
|
ENST00000540732.3:c.930T>G
|
ENSP00000443246.1:p.Ser310=
|
|
ENST00000542943.5:c.741T>G
|
ENSP00000440345.1:p.Ser247=
|
|
ENST00000545787.1:n.456T>G
|
|
|
ENST00000595085.5:c.828T>G
|
ENSP00000471150.2:p.Ser276=
|
|
NM_000709.3:c.828T>G
|
NP_000700.1:p.Ser276=
|
|
NM_001164783.1:c.828T>G
|
NP_001158255.1:p.Ser276=
|
|
NM_000709.4:c.828T>G
MANE Select
|
NP_000700.1:p.Ser276=
|
|
NM_001164783.2:c.828T>G
|
NP_001158255.1:p.Ser276=
|
|