ENST00000311907.10:c.642C>G
MANE Select
|
ENSP00000308541.5:p.Val214=
|
|
ENST00000311907.9:c.642C>G
|
ENSP00000308541.5:p.Val214=
|
|
ENST00000442468.1:c.612C>G
|
ENSP00000387413.1:p.Val204=
|
|
ENST00000490274.1:n.422C>G
|
|
|
ENST00000530231.5:c.642C>G
|
ENSP00000433907.1:p.Val214=
|
|
NM_000506.3:c.642C>G
|
NP_000497.1:p.Val214=
|
|
NM_000506.4:c.642C>G , LRG_551t1:c.642C>G
|
NP_000497.1:p.Val214=
|
|
NM_001311257.1:c.594C>G
|
NP_001298186.1:p.Val198=
|
|
XR_428840.2:n.686C>G
|
|
|
XR_428840.4:n.677C>G
|
|
|
NM_000506.5:c.642C>G
MANE Select
|
NP_000497.1:p.Val214=
|
|
NM_001311257.2:c.594C>G
|
NP_001298186.1:p.Val198=
|
|