ENST00000328300.11:c.4532C>G
MANE Select
|
ENSP00000331902.7:p.Thr1511Arg
|
|
ENST00000361603.7:c.4514C>G
|
ENSP00000354505.2:p.Thr1505Arg
|
|
ENST00000510690.2:n.1026C>G
|
|
|
ENST00000328300.10:c.4532C>G
|
ENSP00000331902.6:p.Thr1511Arg
|
|
ENST00000361603.6:c.4514C>G
|
ENSP00000354505.2:p.Thr1505Arg
|
|
ENST00000515658.1:c.325-3546C>G
|
|
|
NM_000495.4:c.4514C>G
|
NP_000486.1:p.Thr1505Arg
|
|
NM_033380.2:c.4532C>G
|
NP_203699.1:p.Thr1511Arg
|
|
XM_005262070.2:c.4523C>G
|
XP_005262127.1:p.Thr1508Arg
|
|
XM_006724616.2:c.4532C>G
|
XP_006724679.1:p.Thr1511Arg
|
|
XM_011530849.1:c.4208C>G
|
XP_011529151.1:p.Thr1403Arg
|
|
XM_011530851.1:c.2105C>G
|
XP_011529153.1:p.Thr702Arg
|
|
XM_011530849.2:c.4547C>G
|
XP_011529151.2:p.Thr1516Arg
|
|
XM_017029259.2:c.4538C>G
|
XP_016884748.1:p.Thr1513Arg
|
|
XM_017029260.1:c.4529C>G
|
XP_016884749.1:p.Thr1510Arg
|
|
XM_017029263.2:c.2867C>G
|
XP_016884752.1:p.Thr956Arg
|
|
NM_000495.5:c.4514C>G
|
NP_000486.1:p.Thr1505Arg
|
|
NM_033380.3:c.4532C>G
MANE Select
|
NP_203699.1:p.Thr1511Arg
|
|