ENST00000328300.11:c.4553G>C
MANE Select
|
ENSP00000331902.7:p.Arg1518Pro
|
|
ENST00000361603.7:c.4535G>C
|
ENSP00000354505.2:p.Arg1512Pro
|
|
ENST00000510690.2:n.1047G>C
|
|
|
ENST00000328300.10:c.4553G>C
|
ENSP00000331902.6:p.Arg1518Pro
|
|
ENST00000361603.6:c.4535G>C
|
ENSP00000354505.2:p.Arg1512Pro
|
|
ENST00000515658.1:c.325-3525G>C
|
|
|
NM_000495.4:c.4535G>C
|
NP_000486.1:p.Arg1512Pro
|
|
NM_033380.2:c.4553G>C
|
NP_203699.1:p.Arg1518Pro
|
|
XM_005262070.2:c.4544G>C
|
XP_005262127.1:p.Arg1515Pro
|
|
XM_006724616.2:c.4553G>C
|
XP_006724679.1:p.Arg1518Pro
|
|
XM_011530849.1:c.4229G>C
|
XP_011529151.1:p.Arg1410Pro
|
|
XM_011530851.1:c.2126G>C
|
XP_011529153.1:p.Arg709Pro
|
|
XM_011530849.2:c.4568G>C
|
XP_011529151.2:p.Arg1523Pro
|
|
XM_017029259.2:c.4559G>C
|
XP_016884748.1:p.Arg1520Pro
|
|
XM_017029260.1:c.4550G>C
|
XP_016884749.1:p.Arg1517Pro
|
|
XM_017029263.2:c.2888G>C
|
XP_016884752.1:p.Arg963Pro
|
|
NM_000495.5:c.4535G>C
|
NP_000486.1:p.Arg1512Pro
|
|
NM_033380.3:c.4553G>C
MANE Select
|
NP_203699.1:p.Arg1518Pro
|
|