ENST00000328300.11:c.4319C>G
MANE Select
|
ENSP00000331902.7:p.Thr1440Ser
|
|
ENST00000361603.7:c.4301C>G
|
ENSP00000354505.2:p.Thr1434Ser
|
|
ENST00000510690.2:n.813C>G
|
|
|
ENST00000328300.10:c.4319C>G
|
ENSP00000331902.6:p.Thr1440Ser
|
|
ENST00000361603.6:c.4301C>G
|
ENSP00000354505.2:p.Thr1434Ser
|
|
ENST00000489230.1:n.722C>G
|
|
|
ENST00000515658.1:c.115C>G
|
|
|
NM_000495.4:c.4301C>G
|
NP_000486.1:p.Thr1434Ser
|
|
NM_033380.2:c.4319C>G
|
NP_203699.1:p.Thr1440Ser
|
|
XM_005262070.2:c.4310C>G
|
XP_005262127.1:p.Thr1437Ser
|
|
XM_006724616.2:c.4319C>G
|
XP_006724679.1:p.Thr1440Ser
|
|
XM_011530849.1:c.3995C>G
|
XP_011529151.1:p.Thr1332Ser
|
|
XM_011530851.1:c.1892C>G
|
XP_011529153.1:p.Thr631Ser
|
|
XM_011530849.2:c.4334C>G
|
XP_011529151.2:p.Thr1445Ser
|
|
XM_017029259.2:c.4325C>G
|
XP_016884748.1:p.Thr1442Ser
|
|
XM_017029260.1:c.4316C>G
|
XP_016884749.1:p.Thr1439Ser
|
|
XM_017029263.2:c.2654C>G
|
XP_016884752.1:p.Thr885Ser
|
|
NM_000495.5:c.4301C>G
|
NP_000486.1:p.Thr1434Ser
|
|
NM_033380.3:c.4319C>G
MANE Select
|
NP_203699.1:p.Thr1440Ser
|
|