ENST00000311907.10:c.591A>C
MANE Select
|
ENSP00000308541.5:p.Pro197=
|
|
ENST00000311907.9:c.591A>C
|
ENSP00000308541.5:p.Pro197=
|
|
ENST00000442468.1:c.561A>C
|
ENSP00000387413.1:p.Pro187=
|
|
ENST00000490274.1:n.371A>C
|
|
|
ENST00000530231.5:c.591A>C
|
ENSP00000433907.1:p.Pro197=
|
|
NM_000506.3:c.591A>C
|
NP_000497.1:p.Pro197=
|
|
NM_000506.4:c.591A>C , LRG_551t1:c.591A>C
|
NP_000497.1:p.Pro197=
|
|
NM_001311257.1:c.543A>C
|
NP_001298186.1:p.Pro181=
|
|
XR_428840.2:n.635A>C
|
|
|
XR_428840.4:n.626A>C
|
|
|
NM_000506.5:c.591A>C
MANE Select
|
NP_000497.1:p.Pro197=
|
|
NM_001311257.2:c.543A>C
|
NP_001298186.1:p.Pro181=
|
|