ENST00000328300.11:c.4046C>A
MANE Select
|
ENSP00000331902.7:p.Ser1349Ter
|
|
ENST00000361603.7:c.4028C>A
|
ENSP00000354505.2:p.Ser1343Ter
|
|
ENST00000510690.2:n.540C>A
|
|
|
ENST00000328300.10:c.4046C>A
|
ENSP00000331902.6:p.Ser1349Ter
|
|
ENST00000361603.6:c.4028C>A
|
ENSP00000354505.2:p.Ser1343Ter
|
|
ENST00000489230.1:n.449C>A
|
|
|
NM_000495.4:c.4028C>A
|
NP_000486.1:p.Ser1343Ter
|
|
NM_033380.2:c.4046C>A
|
NP_203699.1:p.Ser1349Ter
|
|
XM_005262070.2:c.4037C>A
|
XP_005262127.1:p.Ser1346Ter
|
|
XM_006724616.2:c.4046C>A
|
XP_006724679.1:p.Ser1349Ter
|
|
XM_011530849.1:c.3722C>A
|
XP_011529151.1:p.Ser1241Ter
|
|
XM_011530851.1:c.1619C>A
|
XP_011529153.1:p.Ser540Ter
|
|
XM_011530849.2:c.4061C>A
|
XP_011529151.2:p.Ser1354Ter
|
|
XM_017029259.2:c.4052C>A
|
XP_016884748.1:p.Ser1351Ter
|
|
XM_017029260.1:c.4043C>A
|
XP_016884749.1:p.Ser1348Ter
|
|
XM_017029263.2:c.2381C>A
|
XP_016884752.1:p.Ser794Ter
|
|
NM_000495.5:c.4028C>A
|
NP_000486.1:p.Ser1343Ter
|
|
NM_033380.3:c.4046C>A
MANE Select
|
NP_203699.1:p.Ser1349Ter
|
|