ENST00000311907.10:c.699C>T
MANE Select
|
ENSP00000308541.5:p.Pro233=
|
|
ENST00000311907.9:c.699C>T
|
ENSP00000308541.5:p.Pro233=
|
|
ENST00000442468.1:c.669C>T
|
ENSP00000387413.1:p.Pro223=
|
|
ENST00000490274.1:n.479C>T
|
|
|
ENST00000530231.5:c.699C>T
|
ENSP00000433907.1:p.Pro233=
|
|
NM_000506.3:c.699C>T
|
NP_000497.1:p.Pro233=
|
|
NM_000506.4:c.699C>T , LRG_551t1:c.699C>T
|
NP_000497.1:p.Pro233=
|
|
NM_001311257.1:c.651C>T
|
NP_001298186.1:p.Pro217=
|
|
XR_428840.2:n.743C>T
|
|
|
XR_428840.4:n.734C>T
|
|
|
NM_000506.5:c.699C>T
MANE Select
|
NP_000497.1:p.Pro233=
|
|
NM_001311257.2:c.651C>T
|
NP_001298186.1:p.Pro217=
|
|