ENST00000328300.11:c.4720G>C
MANE Select
|
ENSP00000331902.7:p.Glu1574Gln
|
|
ENST00000361603.7:c.4702G>C
|
ENSP00000354505.2:p.Glu1568Gln
|
|
ENST00000510690.2:n.1214G>C
|
|
|
ENST00000644079.1:n.1206G>C
|
|
|
ENST00000328300.10:c.4720G>C
|
ENSP00000331902.6:p.Glu1574Gln
|
|
ENST00000361603.6:c.4702G>C
|
ENSP00000354505.2:p.Glu1568Gln
|
|
ENST00000504541.1:c.118G>C
|
ENSP00000424845.1:p.Glu40Gln
|
|
ENST00000515658.1:c.325-1477G>C
|
|
|
NM_000495.4:c.4702G>C
|
NP_000486.1:p.Glu1568Gln
|
|
NM_033380.2:c.4720G>C
|
NP_203699.1:p.Glu1574Gln
|
|
XM_005262070.2:c.4711G>C
|
XP_005262127.1:p.Glu1571Gln
|
|
XM_006724616.2:c.4720G>C
|
XP_006724679.1:p.Glu1574Gln
|
|
XM_011530849.1:c.4396G>C
|
XP_011529151.1:p.Glu1466Gln
|
|
XM_011530851.1:c.2293G>C
|
XP_011529153.1:p.Glu765Gln
|
|
XM_011530849.2:c.4735G>C
|
XP_011529151.2:p.Glu1579Gln
|
|
XM_017029259.2:c.4726G>C
|
XP_016884748.1:p.Glu1576Gln
|
|
XM_017029260.1:c.4717G>C
|
XP_016884749.1:p.Glu1573Gln
|
|
XM_017029263.2:c.3055G>C
|
XP_016884752.1:p.Glu1019Gln
|
|
NM_000495.5:c.4702G>C
|
NP_000486.1:p.Glu1568Gln
|
|
NM_033380.3:c.4720G>C
MANE Select
|
NP_203699.1:p.Glu1574Gln
|
|