ENST00000328300.11:c.4301T>C
MANE Select
|
ENSP00000331902.7:p.Leu1434Pro
|
|
ENST00000361603.7:c.4283T>C
|
ENSP00000354505.2:p.Leu1428Pro
|
|
ENST00000510690.2:n.795T>C
|
|
|
ENST00000328300.10:c.4301T>C
|
ENSP00000331902.6:p.Leu1434Pro
|
|
ENST00000361603.6:c.4283T>C
|
ENSP00000354505.2:p.Leu1428Pro
|
|
ENST00000489230.1:n.704T>C
|
|
|
ENST00000515658.1:c.97T>C
|
|
|
NM_000495.4:c.4283T>C
|
NP_000486.1:p.Leu1428Pro
|
|
NM_033380.2:c.4301T>C
|
NP_203699.1:p.Leu1434Pro
|
|
XM_005262070.2:c.4292T>C
|
XP_005262127.1:p.Leu1431Pro
|
|
XM_006724616.2:c.4301T>C
|
XP_006724679.1:p.Leu1434Pro
|
|
XM_011530849.1:c.3977T>C
|
XP_011529151.1:p.Leu1326Pro
|
|
XM_011530851.1:c.1874T>C
|
XP_011529153.1:p.Leu625Pro
|
|
XM_011530849.2:c.4316T>C
|
XP_011529151.2:p.Leu1439Pro
|
|
XM_017029259.2:c.4307T>C
|
XP_016884748.1:p.Leu1436Pro
|
|
XM_017029260.1:c.4298T>C
|
XP_016884749.1:p.Leu1433Pro
|
|
XM_017029263.2:c.2636T>C
|
XP_016884752.1:p.Leu879Pro
|
|
NM_000495.5:c.4283T>C
|
NP_000486.1:p.Leu1428Pro
|
|
NM_033380.3:c.4301T>C
MANE Select
|
NP_203699.1:p.Leu1434Pro
|
|