ENST00000328300.11:c.5007A>T
MANE Select
|
ENSP00000331902.7:p.Ser1669=
|
|
ENST00000361603.7:c.4989A>T
|
ENSP00000354505.2:p.Ser1663=
|
|
ENST00000510690.2:n.1501A>T
|
|
|
ENST00000644079.1:n.2695A>T
|
|
|
ENST00000328300.10:c.5007A>T
|
ENSP00000331902.6:p.Ser1669=
|
|
ENST00000361603.6:c.4989A>T
|
ENSP00000354505.2:p.Ser1663=
|
|
ENST00000504541.1:c.232A>T
|
ENSP00000424845.1:n.232A>T
|
|
ENST00000515658.1:c.337A>T
|
|
|
NM_000495.4:c.4989A>T
|
NP_000486.1:p.Ser1663=
|
|
NM_033380.2:c.5007A>T
|
NP_203699.1:p.Ser1669=
|
|
XM_005262070.2:c.4998A>T
|
XP_005262127.1:p.Ser1666=
|
|
XM_006724616.2:c.5007A>T
|
XP_006724679.1:p.Ser1669=
|
|
XM_011530849.1:c.4683A>T
|
XP_011529151.1:p.Ser1561=
|
|
XM_011530851.1:c.2580A>T
|
XP_011529153.1:p.Ser860=
|
|
XM_011530849.2:c.5022A>T
|
XP_011529151.2:p.Ser1674=
|
|
XM_017029259.2:c.5013A>T
|
XP_016884748.1:p.Ser1671=
|
|
XM_017029260.1:c.5004A>T
|
XP_016884749.1:p.Ser1668=
|
|
XM_017029263.2:c.3342A>T
|
XP_016884752.1:p.Ser1114=
|
|
NM_000495.5:c.4989A>T
|
NP_000486.1:p.Ser1663=
|
|
NM_033380.3:c.5007A>T
MANE Select
|
NP_203699.1:p.Ser1669=
|
|