ENST00000311907.10:c.787C>A
MANE Select
|
ENSP00000308541.5:p.Arg263Ser
|
|
ENST00000311907.9:c.787C>A
|
ENSP00000308541.5:p.Arg263Ser
|
|
ENST00000442468.1:c.757C>A
|
ENSP00000387413.1:p.Arg253Ser
|
|
ENST00000530231.5:c.787C>A
|
ENSP00000433907.1:p.Arg263Ser
|
|
NM_000506.3:c.787C>A
|
NP_000497.1:p.Arg263Ser
|
|
NM_000506.4:c.787C>A , LRG_551t1:c.787C>A
|
NP_000497.1:p.Arg263Ser
|
|
NM_001311257.1:c.739C>A
|
NP_001298186.1:p.Arg247Ser
|
|
XR_428840.2:n.831C>A
|
|
|
XR_428840.4:n.822C>A
|
|
|
NM_000506.5:c.787C>A
MANE Select
|
NP_000497.1:p.Arg263Ser
|
|
NM_001311257.2:c.739C>A
|
NP_001298186.1:p.Arg247Ser
|
|