ENST00000328300.11:c.4384T>A
MANE Select
|
ENSP00000331902.7:p.Ser1462Thr
|
|
ENST00000361603.7:c.4366T>A
|
ENSP00000354505.2:p.Ser1456Thr
|
|
ENST00000510690.2:n.878T>A
|
|
|
ENST00000328300.10:c.4384T>A
|
ENSP00000331902.6:p.Ser1462Thr
|
|
ENST00000361603.6:c.4366T>A
|
ENSP00000354505.2:p.Ser1456Thr
|
|
ENST00000515658.1:c.180T>A
|
|
|
NM_000495.4:c.4366T>A
|
NP_000486.1:p.Ser1456Thr
|
|
NM_033380.2:c.4384T>A
|
NP_203699.1:p.Ser1462Thr
|
|
XM_005262070.2:c.4375T>A
|
XP_005262127.1:p.Ser1459Thr
|
|
XM_006724616.2:c.4384T>A
|
XP_006724679.1:p.Ser1462Thr
|
|
XM_011530849.1:c.4060T>A
|
XP_011529151.1:p.Ser1354Thr
|
|
XM_011530851.1:c.1957T>A
|
XP_011529153.1:p.Ser653Thr
|
|
XM_011530849.2:c.4399T>A
|
XP_011529151.2:p.Ser1467Thr
|
|
XM_017029259.2:c.4390T>A
|
XP_016884748.1:p.Ser1464Thr
|
|
XM_017029260.1:c.4381T>A
|
XP_016884749.1:p.Ser1461Thr
|
|
XM_017029263.2:c.2719T>A
|
XP_016884752.1:p.Ser907Thr
|
|
NM_000495.5:c.4366T>A
|
NP_000486.1:p.Ser1456Thr
|
|
NM_033380.3:c.4384T>A
MANE Select
|
NP_203699.1:p.Ser1462Thr
|
|