ENST00000328300.11:c.4939T>C
MANE Select
|
ENSP00000331902.7:p.Tyr1647His
|
|
ENST00000361603.7:c.4921T>C
|
ENSP00000354505.2:p.Tyr1641His
|
|
ENST00000510690.2:n.1433T>C
|
|
|
ENST00000644079.1:n.1770T>C
|
|
|
ENST00000328300.10:c.4939T>C
|
ENSP00000331902.6:p.Tyr1647His
|
|
ENST00000361603.6:c.4921T>C
|
ENSP00000354505.2:p.Tyr1641His
|
|
ENST00000504541.1:c.219+463T>C
|
ENSP00000424845.1:n.219+463T>C
|
|
ENST00000515658.1:c.325-913T>C
|
|
|
NM_000495.4:c.4921T>C
|
NP_000486.1:p.Tyr1641His
|
|
NM_033380.2:c.4939T>C
|
NP_203699.1:p.Tyr1647His
|
|
XM_005262070.2:c.4930T>C
|
XP_005262127.1:p.Tyr1644His
|
|
XM_006724616.2:c.4939T>C
|
XP_006724679.1:p.Tyr1647His
|
|
XM_011530849.1:c.4615T>C
|
XP_011529151.1:p.Tyr1539His
|
|
XM_011530851.1:c.2512T>C
|
XP_011529153.1:p.Tyr838His
|
|
XM_011530849.2:c.4954T>C
|
XP_011529151.2:p.Tyr1652His
|
|
XM_017029259.2:c.4945T>C
|
XP_016884748.1:p.Tyr1649His
|
|
XM_017029260.1:c.4936T>C
|
XP_016884749.1:p.Tyr1646His
|
|
XM_017029263.2:c.3274T>C
|
XP_016884752.1:p.Tyr1092His
|
|
NM_000495.5:c.4921T>C
|
NP_000486.1:p.Tyr1641His
|
|
NM_033380.3:c.4939T>C
MANE Select
|
NP_203699.1:p.Tyr1647His
|
|