ENST00000311907.10:c.582G>C
MANE Select
|
ENSP00000308541.5:p.Ala194=
|
|
ENST00000311907.9:c.582G>C
|
ENSP00000308541.5:p.Ala194=
|
|
ENST00000442468.1:c.552G>C
|
ENSP00000387413.1:p.Ala184=
|
|
ENST00000490274.1:n.362G>C
|
|
|
ENST00000530231.5:c.582G>C
|
ENSP00000433907.1:p.Ala194=
|
|
NM_000506.3:c.582G>C
|
NP_000497.1:p.Ala194=
|
|
NM_000506.4:c.582G>C , LRG_551t1:c.582G>C
|
NP_000497.1:p.Ala194=
|
|
NM_001311257.1:c.534G>C
|
NP_001298186.1:p.Ala178=
|
|
XR_428840.2:n.626G>C
|
|
|
XR_428840.4:n.617G>C
|
|
|
NM_000506.5:c.582G>C
MANE Select
|
NP_000497.1:p.Ala194=
|
|
NM_001311257.2:c.534G>C
|
NP_001298186.1:p.Ala178=
|
|