ENST00000328300.11:c.4915C>T
MANE Select
|
ENSP00000331902.7:p.His1639Tyr
|
|
ENST00000361603.7:c.4897C>T
|
ENSP00000354505.2:p.His1633Tyr
|
|
ENST00000510690.2:n.1409C>T
|
|
|
ENST00000644079.1:n.1746C>T
|
|
|
ENST00000328300.10:c.4915C>T
|
ENSP00000331902.6:p.His1639Tyr
|
|
ENST00000361603.6:c.4897C>T
|
ENSP00000354505.2:p.His1633Tyr
|
|
ENST00000504541.1:c.219+439C>T
|
ENSP00000424845.1:n.219+439C>T
|
|
ENST00000515658.1:c.325-937C>T
|
|
|
NM_000495.4:c.4897C>T
|
NP_000486.1:p.His1633Tyr
|
|
NM_033380.2:c.4915C>T
|
NP_203699.1:p.His1639Tyr
|
|
XM_005262070.2:c.4906C>T
|
XP_005262127.1:p.His1636Tyr
|
|
XM_006724616.2:c.4915C>T
|
XP_006724679.1:p.His1639Tyr
|
|
XM_011530849.1:c.4591C>T
|
XP_011529151.1:p.His1531Tyr
|
|
XM_011530851.1:c.2488C>T
|
XP_011529153.1:p.His830Tyr
|
|
XM_011530849.2:c.4930C>T
|
XP_011529151.2:p.His1644Tyr
|
|
XM_017029259.2:c.4921C>T
|
XP_016884748.1:p.His1641Tyr
|
|
XM_017029260.1:c.4912C>T
|
XP_016884749.1:p.His1638Tyr
|
|
XM_017029263.2:c.3250C>T
|
XP_016884752.1:p.His1084Tyr
|
|
NM_000495.5:c.4897C>T
|
NP_000486.1:p.His1633Tyr
|
|
NM_033380.3:c.4915C>T
MANE Select
|
NP_203699.1:p.His1639Tyr
|
|