|
NM_016169.4:c.1309G>A
MANE Select
|
NP_057253.2:p.Glu437Lys
|
|
ENST00000369902.8:c.1309G>A
MANE Select
|
ENSP00000358918.4:p.Glu437Lys
|
|
NM_016169.3:c.1309G>A , LRG_521t1:c.1309G>A
|
NP_057253.2:p.Glu437Lys
|
|
ENST00000369902.7:c.1309G>A
|
ENSP00000358918.3:p.Glu437Lys
|
|
XM_011539858.1:c.1438G>A
|
XP_011538160.1:p.Glu480Lys
|
|
XM_011539858.3:c.1438G>A
|
XP_011538160.1:p.Glu480Lys
|
|
XM_011539859.1:c.1438G>A
|
XP_011538161.1:p.Glu480Lys
|
|
XM_011539860.1:c.1435G>A
|
XP_011538162.1:p.Glu479Lys
|
|
XM_011539860.3:c.1435G>A
|
XP_011538162.1:p.Glu479Lys
|
|
XM_011539861.1:c.1312G>A
|
XP_011538163.1:p.Glu438Lys
|
|
XM_011539861.3:c.1312G>A
|
XP_011538163.1:p.Glu438Lys
|
|
XM_011539862.1:c.1360G>A
|
XP_011538164.1:p.Glu454Lys
|
|
XM_011539863.1:c.1264G>A
|
XP_011538165.1:p.Glu422Lys
|
|
XM_011539863.3:c.1264G>A
|
XP_011538165.1:p.Glu422Lys
|
|
XM_017016323.1:c.1360G>A
|
XP_016871812.1:p.Glu454Lys
|