ENST00000357578.8:c.1259T>A
MANE Select
|
ENSP00000350191.3:p.Phe420Tyr
|
|
ENST00000479394.2:n.374T>A
|
|
|
ENST00000672352.1:c.878T>A
|
ENSP00000500876.1:p.Phe293Tyr
|
|
ENST00000672652.1:c.1222T>A
|
|
|
ENST00000348925.2:c.1298T>A
|
ENSP00000314649.3:p.Phe433Tyr
|
|
ENST00000357578.7:c.1259T>A
|
ENSP00000350191.3:p.Phe420Tyr
|
|
ENST00000479394.1:n.374T>A
|
|
|
ENST00000491546.5:c.1175T>A
|
ENSP00000417687.1:p.Phe392Tyr
|
|
NM_001080.3:c.1259T>A
MANE Select
|
NP_001071.1:p.Phe420Tyr
|
|
NM_170740.1:c.1298T>A
|
NP_733936.1:p.Phe433Tyr
|
|
NM_001368954.1:c.1115T>A
|
NP_001355883.1:p.Phe372Tyr
|
|