ENST00000269980.7:c.1276T>G
MANE Select
|
ENSP00000269980.2:p.Ser426Ala
|
|
ENST00000269980.6:c.1276T>G
|
ENSP00000269980.2:p.Ser426Ala
|
|
ENST00000457836.6:c.1285T>G
|
ENSP00000416000.2:p.Ser429Ala
|
|
ENST00000540732.3:c.1378T>G
|
ENSP00000443246.1:p.Ser460Ala
|
|
ENST00000544905.1:c.106T>G
|
|
|
ENST00000595085.5:c.922+1849T>G
|
ENSP00000471150.2:n.922+1849T>G
|
|
NM_000709.3:c.1276T>G
|
NP_000700.1:p.Ser426Ala
|
|
NM_001164783.1:c.1273T>G
|
NP_001158255.1:p.Ser425Ala
|
|
NM_000709.4:c.1276T>G
MANE Select
|
NP_000700.1:p.Ser426Ala
|
|
NM_001164783.2:c.1273T>G
|
NP_001158255.1:p.Ser425Ala
|
|