ENST00000328300.11:c.4974A>G
MANE Select
|
ENSP00000331902.7:p.Val1658=
|
|
ENST00000361603.7:c.4956A>G
|
ENSP00000354505.2:p.Val1652=
|
|
ENST00000510690.2:n.1468A>G
|
|
|
ENST00000644079.1:n.1805A>G
|
|
|
ENST00000328300.10:c.4974A>G
|
ENSP00000331902.6:p.Val1658=
|
|
ENST00000361603.6:c.4956A>G
|
ENSP00000354505.2:p.Val1652=
|
|
ENST00000504541.1:c.219+498A>G
|
ENSP00000424845.1:n.219+498A>G
|
|
ENST00000515658.1:c.325-878A>G
|
|
|
NM_000495.4:c.4956A>G
|
NP_000486.1:p.Val1652=
|
|
NM_033380.2:c.4974A>G
|
NP_203699.1:p.Val1658=
|
|
XM_005262070.2:c.4965A>G
|
XP_005262127.1:p.Val1655=
|
|
XM_006724616.2:c.4974A>G
|
XP_006724679.1:p.Val1658=
|
|
XM_011530849.1:c.4650A>G
|
XP_011529151.1:p.Val1550=
|
|
XM_011530851.1:c.2547A>G
|
XP_011529153.1:p.Val849=
|
|
XM_011530849.2:c.4989A>G
|
XP_011529151.2:p.Val1663=
|
|
XM_017029259.2:c.4980A>G
|
XP_016884748.1:p.Val1660=
|
|
XM_017029260.1:c.4971A>G
|
XP_016884749.1:p.Val1657=
|
|
XM_017029263.2:c.3309A>G
|
XP_016884752.1:p.Val1103=
|
|
NM_000495.5:c.4956A>G
|
NP_000486.1:p.Val1652=
|
|
NM_033380.3:c.4974A>G
MANE Select
|
NP_203699.1:p.Val1658=
|
|