ENST00000328300.11:c.4125C>G
MANE Select
|
ENSP00000331902.7:p.Ile1375Met
|
|
ENST00000361603.7:c.4107C>G
|
ENSP00000354505.2:p.Ile1369Met
|
|
ENST00000510690.2:n.619C>G
|
|
|
ENST00000328300.10:c.4125C>G
|
ENSP00000331902.6:p.Ile1375Met
|
|
ENST00000361603.6:c.4107C>G
|
ENSP00000354505.2:p.Ile1369Met
|
|
ENST00000489230.1:n.528C>G
|
|
|
NM_000495.4:c.4107C>G
|
NP_000486.1:p.Ile1369Met
|
|
NM_033380.2:c.4125C>G
|
NP_203699.1:p.Ile1375Met
|
|
XM_005262070.2:c.4116C>G
|
XP_005262127.1:p.Ile1372Met
|
|
XM_006724616.2:c.4125C>G
|
XP_006724679.1:p.Ile1375Met
|
|
XM_011530849.1:c.3801C>G
|
XP_011529151.1:p.Ile1267Met
|
|
XM_011530851.1:c.1698C>G
|
XP_011529153.1:p.Ile566Met
|
|
XM_011530849.2:c.4140C>G
|
XP_011529151.2:p.Ile1380Met
|
|
XM_017029259.2:c.4131C>G
|
XP_016884748.1:p.Ile1377Met
|
|
XM_017029260.1:c.4122C>G
|
XP_016884749.1:p.Ile1374Met
|
|
XM_017029263.2:c.2460C>G
|
XP_016884752.1:p.Ile820Met
|
|
NM_000495.5:c.4107C>G
|
NP_000486.1:p.Ile1369Met
|
|
NM_033380.3:c.4125C>G
MANE Select
|
NP_203699.1:p.Ile1375Met
|
|