ENST00000404085.7:c.659C>A
MANE Select
|
ENSP00000384008.3:p.Ser220Tyr
|
|
ENST00000404261.9:c.659C>A
|
ENSP00000384753.6:p.Ser220Tyr
|
|
ENST00000594072.6:c.659C>A
|
ENSP00000468845.4:p.Ser220Tyr
|
|
ENST00000651416.1:n.876C>A
|
|
|
ENST00000652132.1:c.626C>A
|
ENSP00000498416.1:p.Ser209Tyr
|
|
ENST00000394458.7:c.821C>A
|
ENSP00000377971.4:p.Ser274Tyr
|
|
ENST00000404085.5:c.*558C>A
|
ENSP00000384008.2:n.*558C>A
|
|
ENST00000404261.8:c.821C>A
|
ENSP00000384753.5:p.Ser274Tyr
|
|
ENST00000594072.5:c.821C>A
|
ENSP00000468845.3:p.Ser274Tyr
|
|
ENST00000596626.1:n.772C>A
|
|
|
ENST00000598347.2:c.661C>A
|
|
|
NM_001278443.1:c.788C>A
|
NP_001265372.1:p.Ser263Tyr
|
|
NM_001278444.1:c.821C>A
|
NP_001265373.1:p.Ser274Tyr
|
|
NM_001278445.1:c.725C>A
|
NP_001265374.1:p.Ser242Tyr
|
|
NM_152363.5:c.821C>A
|
NP_689576.5:p.Ser274Tyr
|
|
NR_103530.1:n.935C>A
|
|
|
NM_001278443.2:c.626C>A
|
NP_001265372.2:p.Ser209Tyr
|
|
NM_001278444.2:c.659C>A
|
NP_001265373.2:p.Ser220Tyr
|
|
NM_001278445.2:c.617C>A
|
NP_001265374.2:p.Ser206Tyr
|
|
NM_152363.6:c.659C>A
MANE Select
|
NP_689576.6:p.Ser220Tyr
|
|
NR_103530.2:n.679C>A
|
|
|