ENST00000328300.11:c.4788G>C
MANE Select
|
ENSP00000331902.7:p.Trp1596Cys
|
|
ENST00000361603.7:c.4770G>C
|
ENSP00000354505.2:p.Trp1590Cys
|
|
ENST00000510690.2:n.1282G>C
|
|
|
ENST00000644079.1:n.1274G>C
|
|
|
ENST00000328300.10:c.4788G>C
|
ENSP00000331902.6:p.Trp1596Cys
|
|
ENST00000361603.6:c.4770G>C
|
ENSP00000354505.2:p.Trp1590Cys
|
|
ENST00000504541.1:c.186G>C
|
ENSP00000424845.1:p.Trp62Cys
|
|
ENST00000515658.1:c.325-1409G>C
|
|
|
NM_000495.4:c.4770G>C
|
NP_000486.1:p.Trp1590Cys
|
|
NM_033380.2:c.4788G>C
|
NP_203699.1:p.Trp1596Cys
|
|
XM_005262070.2:c.4779G>C
|
XP_005262127.1:p.Trp1593Cys
|
|
XM_006724616.2:c.4788G>C
|
XP_006724679.1:p.Trp1596Cys
|
|
XM_011530849.1:c.4464G>C
|
XP_011529151.1:p.Trp1488Cys
|
|
XM_011530851.1:c.2361G>C
|
XP_011529153.1:p.Trp787Cys
|
|
XM_011530849.2:c.4803G>C
|
XP_011529151.2:p.Trp1601Cys
|
|
XM_017029259.2:c.4794G>C
|
XP_016884748.1:p.Trp1598Cys
|
|
XM_017029260.1:c.4785G>C
|
XP_016884749.1:p.Trp1595Cys
|
|
XM_017029263.2:c.3123G>C
|
XP_016884752.1:p.Trp1041Cys
|
|
NM_000495.5:c.4770G>C
|
NP_000486.1:p.Trp1590Cys
|
|
NM_033380.3:c.4788G>C
MANE Select
|
NP_203699.1:p.Trp1596Cys
|
|