ENST00000328300.11:c.4354T>G
MANE Select
|
ENSP00000331902.7:p.Leu1452Val
|
|
ENST00000361603.7:c.4336T>G
|
ENSP00000354505.2:p.Leu1446Val
|
|
ENST00000510690.2:n.848T>G
|
|
|
ENST00000328300.10:c.4354T>G
|
ENSP00000331902.6:p.Leu1452Val
|
|
ENST00000361603.6:c.4336T>G
|
ENSP00000354505.2:p.Leu1446Val
|
|
ENST00000515658.1:c.150T>G
|
|
|
NM_000495.4:c.4336T>G
|
NP_000486.1:p.Leu1446Val
|
|
NM_033380.2:c.4354T>G
|
NP_203699.1:p.Leu1452Val
|
|
XM_005262070.2:c.4345T>G
|
XP_005262127.1:p.Leu1449Val
|
|
XM_006724616.2:c.4354T>G
|
XP_006724679.1:p.Leu1452Val
|
|
XM_011530849.1:c.4030T>G
|
XP_011529151.1:p.Leu1344Val
|
|
XM_011530851.1:c.1927T>G
|
XP_011529153.1:p.Leu643Val
|
|
XM_011530849.2:c.4369T>G
|
XP_011529151.2:p.Leu1457Val
|
|
XM_017029259.2:c.4360T>G
|
XP_016884748.1:p.Leu1454Val
|
|
XM_017029260.1:c.4351T>G
|
XP_016884749.1:p.Leu1451Val
|
|
XM_017029263.2:c.2689T>G
|
XP_016884752.1:p.Leu897Val
|
|
NM_000495.5:c.4336T>G
|
NP_000486.1:p.Leu1446Val
|
|
NM_033380.3:c.4354T>G
MANE Select
|
NP_203699.1:p.Leu1452Val
|
|