ENST00000328300.11:c.4745T>A
MANE Select
|
ENSP00000331902.7:p.Val1582Asp
|
|
ENST00000361603.7:c.4727T>A
|
ENSP00000354505.2:p.Val1576Asp
|
|
ENST00000510690.2:n.1239T>A
|
|
|
ENST00000644079.1:n.1231T>A
|
|
|
ENST00000328300.10:c.4745T>A
|
ENSP00000331902.6:p.Val1582Asp
|
|
ENST00000361603.6:c.4727T>A
|
ENSP00000354505.2:p.Val1576Asp
|
|
ENST00000504541.1:c.143T>A
|
ENSP00000424845.1:p.Val48Asp
|
|
ENST00000515658.1:c.325-1452T>A
|
|
|
NM_000495.4:c.4727T>A
|
NP_000486.1:p.Val1576Asp
|
|
NM_033380.2:c.4745T>A
|
NP_203699.1:p.Val1582Asp
|
|
XM_005262070.2:c.4736T>A
|
XP_005262127.1:p.Val1579Asp
|
|
XM_006724616.2:c.4745T>A
|
XP_006724679.1:p.Val1582Asp
|
|
XM_011530849.1:c.4421T>A
|
XP_011529151.1:p.Val1474Asp
|
|
XM_011530851.1:c.2318T>A
|
XP_011529153.1:p.Val773Asp
|
|
XM_011530849.2:c.4760T>A
|
XP_011529151.2:p.Val1587Asp
|
|
XM_017029259.2:c.4751T>A
|
XP_016884748.1:p.Val1584Asp
|
|
XM_017029260.1:c.4742T>A
|
XP_016884749.1:p.Val1581Asp
|
|
XM_017029263.2:c.3080T>A
|
XP_016884752.1:p.Val1027Asp
|
|
NM_000495.5:c.4727T>A
|
NP_000486.1:p.Val1576Asp
|
|
NM_033380.3:c.4745T>A
MANE Select
|
NP_203699.1:p.Val1582Asp
|
|