ENST00000328300.11:c.4866C>A
MANE Select
|
ENSP00000331902.7:p.Ser1622=
|
|
ENST00000361603.7:c.4848C>A
|
ENSP00000354505.2:p.Ser1616=
|
|
ENST00000510690.2:n.1360C>A
|
|
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ENST00000644079.1:n.1697C>A
|
|
|
ENST00000328300.10:c.4866C>A
|
ENSP00000331902.6:p.Ser1622=
|
|
ENST00000361603.6:c.4848C>A
|
ENSP00000354505.2:p.Ser1616=
|
|
ENST00000504541.1:c.219+390C>A
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ENSP00000424845.1:n.219+390C>A
|
|
ENST00000515658.1:c.325-986C>A
|
|
|
NM_000495.4:c.4848C>A
|
NP_000486.1:p.Ser1616=
|
|
NM_033380.2:c.4866C>A
|
NP_203699.1:p.Ser1622=
|
|
XM_005262070.2:c.4857C>A
|
XP_005262127.1:p.Ser1619=
|
|
XM_006724616.2:c.4866C>A
|
XP_006724679.1:p.Ser1622=
|
|
XM_011530849.1:c.4542C>A
|
XP_011529151.1:p.Ser1514=
|
|
XM_011530851.1:c.2439C>A
|
XP_011529153.1:p.Ser813=
|
|
XM_011530849.2:c.4881C>A
|
XP_011529151.2:p.Ser1627=
|
|
XM_017029259.2:c.4872C>A
|
XP_016884748.1:p.Ser1624=
|
|
XM_017029260.1:c.4863C>A
|
XP_016884749.1:p.Ser1621=
|
|
XM_017029263.2:c.3201C>A
|
XP_016884752.1:p.Ser1067=
|
|
NM_000495.5:c.4848C>A
|
NP_000486.1:p.Ser1616=
|
|
NM_033380.3:c.4866C>A
MANE Select
|
NP_203699.1:p.Ser1622=
|
|