ENST00000328300.11:c.4780C>T
MANE Select
|
ENSP00000331902.7:p.Gln1594Ter
|
|
ENST00000361603.7:c.4762C>T
|
ENSP00000354505.2:p.Gln1588Ter
|
|
ENST00000510690.2:n.1274C>T
|
|
|
ENST00000644079.1:n.1266C>T
|
|
|
ENST00000328300.10:c.4780C>T
|
ENSP00000331902.6:p.Gln1594Ter
|
|
ENST00000361603.6:c.4762C>T
|
ENSP00000354505.2:p.Gln1588Ter
|
|
ENST00000504541.1:c.178C>T
|
ENSP00000424845.1:p.Gln60Ter
|
|
ENST00000515658.1:c.325-1417C>T
|
|
|
NM_000495.4:c.4762C>T
|
NP_000486.1:p.Gln1588Ter
|
|
NM_033380.2:c.4780C>T
|
NP_203699.1:p.Gln1594Ter
|
|
XM_005262070.2:c.4771C>T
|
XP_005262127.1:p.Gln1591Ter
|
|
XM_006724616.2:c.4780C>T
|
XP_006724679.1:p.Gln1594Ter
|
|
XM_011530849.1:c.4456C>T
|
XP_011529151.1:p.Gln1486Ter
|
|
XM_011530851.1:c.2353C>T
|
XP_011529153.1:p.Gln785Ter
|
|
XM_011530849.2:c.4795C>T
|
XP_011529151.2:p.Gln1599Ter
|
|
XM_017029259.2:c.4786C>T
|
XP_016884748.1:p.Gln1596Ter
|
|
XM_017029260.1:c.4777C>T
|
XP_016884749.1:p.Gln1593Ter
|
|
XM_017029263.2:c.3115C>T
|
XP_016884752.1:p.Gln1039Ter
|
|
NM_000495.5:c.4762C>T
|
NP_000486.1:p.Gln1588Ter
|
|
NM_033380.3:c.4780C>T
MANE Select
|
NP_203699.1:p.Gln1594Ter
|
|