ENST00000311907.10:c.592C>T
MANE Select
|
ENSP00000308541.5:p.Arg198Cys
|
|
ENST00000311907.9:c.592C>T
|
ENSP00000308541.5:p.Arg198Cys
|
|
ENST00000442468.1:c.562C>T
|
ENSP00000387413.1:p.Arg188Cys
|
|
ENST00000490274.1:n.372C>T
|
|
|
ENST00000530231.5:c.592C>T
|
ENSP00000433907.1:p.Arg198Cys
|
|
NM_000506.3:c.592C>T
|
NP_000497.1:p.Arg198Cys
|
|
NM_000506.4:c.592C>T , LRG_551t1:c.592C>T
|
NP_000497.1:p.Arg198Cys
|
|
NM_001311257.1:c.544C>T
|
NP_001298186.1:p.Arg182Cys
|
|
XR_428840.2:n.636C>T
|
|
|
XR_428840.4:n.627C>T
|
|
|
NM_000506.5:c.592C>T
MANE Select
|
NP_000497.1:p.Arg198Cys
|
|
NM_001311257.2:c.544C>T
|
NP_001298186.1:p.Arg182Cys
|
|