ENST00000311907.10:c.649C>T
MANE Select
|
ENSP00000308541.5:p.Arg217Trp
|
|
ENST00000311907.9:c.649C>T
|
ENSP00000308541.5:p.Arg217Trp
|
|
ENST00000442468.1:c.619C>T
|
ENSP00000387413.1:p.Arg207Trp
|
|
ENST00000490274.1:n.429C>T
|
|
|
ENST00000530231.5:c.649C>T
|
ENSP00000433907.1:p.Arg217Trp
|
|
NM_000506.3:c.649C>T
|
NP_000497.1:p.Arg217Trp
|
|
NM_000506.4:c.649C>T , LRG_551t1:c.649C>T
|
NP_000497.1:p.Arg217Trp
|
|
NM_001311257.1:c.601C>T
|
NP_001298186.1:p.Arg201Trp
|
|
XR_428840.2:n.693C>T
|
|
|
XR_428840.4:n.684C>T
|
|
|
NM_000506.5:c.649C>T
MANE Select
|
NP_000497.1:p.Arg217Trp
|
|
NM_001311257.2:c.601C>T
|
NP_001298186.1:p.Arg201Trp
|
|