ENST00000328300.11:c.4842A>G
MANE Select
|
ENSP00000331902.7:p.Glu1614=
|
|
ENST00000361603.7:c.4824A>G
|
ENSP00000354505.2:p.Glu1608=
|
|
ENST00000510690.2:n.1336A>G
|
|
|
ENST00000644079.1:n.1673A>G
|
|
|
ENST00000328300.10:c.4842A>G
|
ENSP00000331902.6:p.Glu1614=
|
|
ENST00000361603.6:c.4824A>G
|
ENSP00000354505.2:p.Glu1608=
|
|
ENST00000504541.1:c.219+366A>G
|
ENSP00000424845.1:n.219+366A>G
|
|
ENST00000515658.1:c.325-1010A>G
|
|
|
NM_000495.4:c.4824A>G
|
NP_000486.1:p.Glu1608=
|
|
NM_033380.2:c.4842A>G
|
NP_203699.1:p.Glu1614=
|
|
XM_005262070.2:c.4833A>G
|
XP_005262127.1:p.Glu1611=
|
|
XM_006724616.2:c.4842A>G
|
XP_006724679.1:p.Glu1614=
|
|
XM_011530849.1:c.4518A>G
|
XP_011529151.1:p.Glu1506=
|
|
XM_011530851.1:c.2415A>G
|
XP_011529153.1:p.Glu805=
|
|
XM_011530849.2:c.4857A>G
|
XP_011529151.2:p.Glu1619=
|
|
XM_017029259.2:c.4848A>G
|
XP_016884748.1:p.Glu1616=
|
|
XM_017029260.1:c.4839A>G
|
XP_016884749.1:p.Glu1613=
|
|
XM_017029263.2:c.3177A>G
|
XP_016884752.1:p.Glu1059=
|
|
NM_000495.5:c.4824A>G
|
NP_000486.1:p.Glu1608=
|
|
NM_033380.3:c.4842A>G
MANE Select
|
NP_203699.1:p.Glu1614=
|
|