ENST00000328300.11:c.4763A>G
MANE Select
|
ENSP00000331902.7:p.Gln1588Arg
|
|
ENST00000361603.7:c.4745A>G
|
ENSP00000354505.2:p.Gln1582Arg
|
|
ENST00000510690.2:n.1257A>G
|
|
|
ENST00000644079.1:n.1249A>G
|
|
|
ENST00000328300.10:c.4763A>G
|
ENSP00000331902.6:p.Gln1588Arg
|
|
ENST00000361603.6:c.4745A>G
|
ENSP00000354505.2:p.Gln1582Arg
|
|
ENST00000504541.1:c.161A>G
|
ENSP00000424845.1:p.Gln54Arg
|
|
ENST00000515658.1:c.325-1434A>G
|
|
|
NM_000495.4:c.4745A>G
|
NP_000486.1:p.Gln1582Arg
|
|
NM_033380.2:c.4763A>G
|
NP_203699.1:p.Gln1588Arg
|
|
XM_005262070.2:c.4754A>G
|
XP_005262127.1:p.Gln1585Arg
|
|
XM_006724616.2:c.4763A>G
|
XP_006724679.1:p.Gln1588Arg
|
|
XM_011530849.1:c.4439A>G
|
XP_011529151.1:p.Gln1480Arg
|
|
XM_011530851.1:c.2336A>G
|
XP_011529153.1:p.Gln779Arg
|
|
XM_011530849.2:c.4778A>G
|
XP_011529151.2:p.Gln1593Arg
|
|
XM_017029259.2:c.4769A>G
|
XP_016884748.1:p.Gln1590Arg
|
|
XM_017029260.1:c.4760A>G
|
XP_016884749.1:p.Gln1587Arg
|
|
XM_017029263.2:c.3098A>G
|
XP_016884752.1:p.Gln1033Arg
|
|
NM_000495.5:c.4745A>G
|
NP_000486.1:p.Gln1582Arg
|
|
NM_033380.3:c.4763A>G
MANE Select
|
NP_203699.1:p.Gln1588Arg
|
|