ENST00000328300.11:c.4328T>A
MANE Select
|
ENSP00000331902.7:p.Leu1443Ter
|
|
ENST00000361603.7:c.4310T>A
|
ENSP00000354505.2:p.Leu1437Ter
|
|
ENST00000510690.2:n.822T>A
|
|
|
ENST00000328300.10:c.4328T>A
|
ENSP00000331902.6:p.Leu1443Ter
|
|
ENST00000361603.6:c.4310T>A
|
ENSP00000354505.2:p.Leu1437Ter
|
|
ENST00000489230.1:n.731T>A
|
|
|
ENST00000515658.1:c.124T>A
|
|
|
NM_000495.4:c.4310T>A
|
NP_000486.1:p.Leu1437Ter
|
|
NM_033380.2:c.4328T>A
|
NP_203699.1:p.Leu1443Ter
|
|
XM_005262070.2:c.4319T>A
|
XP_005262127.1:p.Leu1440Ter
|
|
XM_006724616.2:c.4328T>A
|
XP_006724679.1:p.Leu1443Ter
|
|
XM_011530849.1:c.4004T>A
|
XP_011529151.1:p.Leu1335Ter
|
|
XM_011530851.1:c.1901T>A
|
XP_011529153.1:p.Leu634Ter
|
|
XM_011530849.2:c.4343T>A
|
XP_011529151.2:p.Leu1448Ter
|
|
XM_017029259.2:c.4334T>A
|
XP_016884748.1:p.Leu1445Ter
|
|
XM_017029260.1:c.4325T>A
|
XP_016884749.1:p.Leu1442Ter
|
|
XM_017029263.2:c.2663T>A
|
XP_016884752.1:p.Leu888Ter
|
|
NM_000495.5:c.4310T>A
|
NP_000486.1:p.Leu1437Ter
|
|
NM_033380.3:c.4328T>A
MANE Select
|
NP_203699.1:p.Leu1443Ter
|
|