ENST00000311907.10:c.802G>C
MANE Select
|
ENSP00000308541.5:p.Asp268His
|
|
ENST00000311907.9:c.802G>C
|
ENSP00000308541.5:p.Asp268His
|
|
ENST00000442468.1:c.772G>C
|
ENSP00000387413.1:p.Asp258His
|
|
ENST00000530231.5:c.802G>C
|
ENSP00000433907.1:p.Asp268His
|
|
NM_000506.3:c.802G>C
|
NP_000497.1:p.Asp268His
|
|
NM_000506.4:c.802G>C , LRG_551t1:c.802G>C
|
NP_000497.1:p.Asp268His
|
|
NM_001311257.1:c.754G>C
|
NP_001298186.1:p.Asp252His
|
|
XR_428840.2:n.846G>C
|
|
|
XR_428840.4:n.837G>C
|
|
|
NM_000506.5:c.802G>C
MANE Select
|
NP_000497.1:p.Asp268His
|
|
NM_001311257.2:c.754G>C
|
NP_001298186.1:p.Asp252His
|
|