ENST00000362061.4:c.4747G>A
MANE Select
|
ENSP00000355192.3:p.Glu1583Lys
|
|
ENST00000679417.1:c.*3910G>A
|
ENSP00000506706.1:n.*3910G>A
|
|
ENST00000680051.1:n.1873G>A
|
|
|
ENST00000680059.1:c.*2265G>A
|
ENSP00000504944.1:n.*2265G>A
|
|
ENST00000681078.1:c.*522G>A
|
ENSP00000506645.1:n.*522G>A
|
|
ENST00000681190.1:c.*929G>A
|
ENSP00000506428.1:n.*929G>A
|
|
ENST00000681874.1:c.4687G>A
|
ENSP00000505162.1:p.Glu1563Lys
|
|
ENST00000362061.3:c.4747G>A
|
ENSP00000355192.3:p.Glu1583Lys
|
|
ENST00000367338.7:c.4690G>A
|
ENSP00000356307.3:p.Glu1564Lys
|
|
NM_000069.2:c.4747G>A
|
NP_000060.2:p.Glu1583Lys
|
|
XM_005245478.2:c.4690G>A
|
XP_005245535.1:p.Glu1564Lys
|
|
XM_005245478.3:c.4690G>A
|
XP_005245535.1:p.Glu1564Lys
|
|
NM_000069.3:c.4747G>A
MANE Select
|
NP_000060.2:p.Glu1583Lys
|
|