ENST00000328300.11:c.4508G>A
MANE Select
|
ENSP00000331902.7:p.Arg1503Lys
|
|
ENST00000361603.7:c.4490G>A
|
ENSP00000354505.2:p.Arg1497Lys
|
|
ENST00000510690.2:n.1002G>A
|
|
|
ENST00000328300.10:c.4508G>A
|
ENSP00000331902.6:p.Arg1503Lys
|
|
ENST00000361603.6:c.4490G>A
|
ENSP00000354505.2:p.Arg1497Lys
|
|
ENST00000515658.1:c.304G>A
|
|
|
NM_000495.4:c.4490G>A
|
NP_000486.1:p.Arg1497Lys
|
|
NM_033380.2:c.4508G>A
|
NP_203699.1:p.Arg1503Lys
|
|
XM_005262070.2:c.4499G>A
|
XP_005262127.1:p.Arg1500Lys
|
|
XM_006724616.2:c.4508G>A
|
XP_006724679.1:p.Arg1503Lys
|
|
XM_011530849.1:c.4184G>A
|
XP_011529151.1:p.Arg1395Lys
|
|
XM_011530851.1:c.2081G>A
|
XP_011529153.1:p.Arg694Lys
|
|
XM_011530849.2:c.4523G>A
|
XP_011529151.2:p.Arg1508Lys
|
|
XM_017029259.2:c.4514G>A
|
XP_016884748.1:p.Arg1505Lys
|
|
XM_017029260.1:c.4505G>A
|
XP_016884749.1:p.Arg1502Lys
|
|
XM_017029263.2:c.2843G>A
|
XP_016884752.1:p.Arg948Lys
|
|
NM_000495.5:c.4490G>A
|
NP_000486.1:p.Arg1497Lys
|
|
NM_033380.3:c.4508G>A
MANE Select
|
NP_203699.1:p.Arg1503Lys
|
|