ENST00000311907.10:c.596C>A
MANE Select
|
ENSP00000308541.5:p.Ser199Tyr
|
|
ENST00000311907.9:c.596C>A
|
ENSP00000308541.5:p.Ser199Tyr
|
|
ENST00000442468.1:c.566C>A
|
ENSP00000387413.1:p.Ser189Tyr
|
|
ENST00000490274.1:n.376C>A
|
|
|
ENST00000530231.5:c.596C>A
|
ENSP00000433907.1:p.Ser199Tyr
|
|
NM_000506.3:c.596C>A
|
NP_000497.1:p.Ser199Tyr
|
|
NM_000506.4:c.596C>A , LRG_551t1:c.596C>A
|
NP_000497.1:p.Ser199Tyr
|
|
NM_001311257.1:c.548C>A
|
NP_001298186.1:p.Ser183Tyr
|
|
XR_428840.2:n.640C>A
|
|
|
XR_428840.4:n.631C>A
|
|
|
NM_000506.5:c.596C>A
MANE Select
|
NP_000497.1:p.Ser199Tyr
|
|
NM_001311257.2:c.548C>A
|
NP_001298186.1:p.Ser183Tyr
|
|