ENST00000328300.11:c.4970C>G
MANE Select
|
ENSP00000331902.7:p.Thr1657Ser
|
|
ENST00000361603.7:c.4952C>G
|
ENSP00000354505.2:p.Thr1651Ser
|
|
ENST00000510690.2:n.1464C>G
|
|
|
ENST00000644079.1:n.1801C>G
|
|
|
ENST00000328300.10:c.4970C>G
|
ENSP00000331902.6:p.Thr1657Ser
|
|
ENST00000361603.6:c.4952C>G
|
ENSP00000354505.2:p.Thr1651Ser
|
|
ENST00000504541.1:c.219+494C>G
|
ENSP00000424845.1:n.219+494C>G
|
|
ENST00000515658.1:c.325-882C>G
|
|
|
NM_000495.4:c.4952C>G
|
NP_000486.1:p.Thr1651Ser
|
|
NM_033380.2:c.4970C>G
|
NP_203699.1:p.Thr1657Ser
|
|
XM_005262070.2:c.4961C>G
|
XP_005262127.1:p.Thr1654Ser
|
|
XM_006724616.2:c.4970C>G
|
XP_006724679.1:p.Thr1657Ser
|
|
XM_011530849.1:c.4646C>G
|
XP_011529151.1:p.Thr1549Ser
|
|
XM_011530851.1:c.2543C>G
|
XP_011529153.1:p.Thr848Ser
|
|
XM_011530849.2:c.4985C>G
|
XP_011529151.2:p.Thr1662Ser
|
|
XM_017029259.2:c.4976C>G
|
XP_016884748.1:p.Thr1659Ser
|
|
XM_017029260.1:c.4967C>G
|
XP_016884749.1:p.Thr1656Ser
|
|
XM_017029263.2:c.3305C>G
|
XP_016884752.1:p.Thr1102Ser
|
|
NM_000495.5:c.4952C>G
|
NP_000486.1:p.Thr1651Ser
|
|
NM_033380.3:c.4970C>G
MANE Select
|
NP_203699.1:p.Thr1657Ser
|
|