ENST00000328300.11:c.4922G>T
MANE Select
|
ENSP00000331902.7:p.Arg1641Met
|
|
ENST00000361603.7:c.4904G>T
|
ENSP00000354505.2:p.Arg1635Met
|
|
ENST00000510690.2:n.1416G>T
|
|
|
ENST00000644079.1:n.1753G>T
|
|
|
ENST00000328300.10:c.4922G>T
|
ENSP00000331902.6:p.Arg1641Met
|
|
ENST00000361603.6:c.4904G>T
|
ENSP00000354505.2:p.Arg1635Met
|
|
ENST00000504541.1:c.219+446G>T
|
ENSP00000424845.1:n.219+446G>T
|
|
ENST00000515658.1:c.325-930G>T
|
|
|
NM_000495.4:c.4904G>T
|
NP_000486.1:p.Arg1635Met
|
|
NM_033380.2:c.4922G>T
|
NP_203699.1:p.Arg1641Met
|
|
XM_005262070.2:c.4913G>T
|
XP_005262127.1:p.Arg1638Met
|
|
XM_006724616.2:c.4922G>T
|
XP_006724679.1:p.Arg1641Met
|
|
XM_011530849.1:c.4598G>T
|
XP_011529151.1:p.Arg1533Met
|
|
XM_011530851.1:c.2495G>T
|
XP_011529153.1:p.Arg832Met
|
|
XM_011530849.2:c.4937G>T
|
XP_011529151.2:p.Arg1646Met
|
|
XM_017029259.2:c.4928G>T
|
XP_016884748.1:p.Arg1643Met
|
|
XM_017029260.1:c.4919G>T
|
XP_016884749.1:p.Arg1640Met
|
|
XM_017029263.2:c.3257G>T
|
XP_016884752.1:p.Arg1086Met
|
|
NM_000495.5:c.4904G>T
|
NP_000486.1:p.Arg1635Met
|
|
NM_033380.3:c.4922G>T
MANE Select
|
NP_203699.1:p.Arg1641Met
|
|