|
NM_203475.3:c.1186C>T
MANE Select
|
NP_982301.1:p.Arg396Ter
|
|
ENST00000326194.11:c.1186C>T
MANE Select
|
ENSP00000322304.6:p.Arg396Ter
|
|
NM_001282167.1:c.940C>T
|
NP_001269096.1:p.Arg314Ter
|
|
NM_001282167.2:c.940C>T
|
NP_001269096.1:p.Arg314Ter
|
|
NM_022825.3:c.1153C>T
|
NP_073736.2:p.Arg385Ter
|
|
NM_022825.4:c.1153C>T
|
NP_073736.2:p.Arg385Ter
|
|
NM_203473.2:c.1171C>T
|
NP_982299.1:p.Arg391Ter
|
|
NM_203473.3:c.1171C>T
|
NP_982299.1:p.Arg391Ter
|
|
NM_203474.1:c.1168C>T
|
NP_982300.1:p.Arg390Ter
|
|
NM_203475.2:c.1186C>T
|
NP_982301.1:p.Arg396Ter
|
|
ENST00000326194.10:c.1186C>T
|
ENSP00000322304.6:p.Arg396Ter
|
|
ENST00000355092.4:c.1018C>T
|
ENSP00000347207.4:p.Arg340Ter
|
|
ENST00000355961.8:c.1171C>T
|
ENSP00000348233.4:p.Arg391Ter
|
|
ENST00000359882.8:c.1168C>T
|
ENSP00000352946.4:p.Arg390Ter
|
|
ENST00000361988.7:c.1153C>T
|
ENSP00000354978.3:p.Arg385Ter
|
|
ENST00000367574.8:c.1168C>T
|
ENSP00000356546.5:p.Arg390Ter
|
|
ENST00000367574.9:c.1153C>T
|
ENSP00000356546.6:p.Arg385Ter
|
|
ENST00000472520.5:c.*494C>T
|
ENSP00000419858.1:n.*494C>T
|
|
ENST00000485288.6:c.*821C>T
|
ENSP00000420445.2:n.*821C>T
|
|
ENST00000485288.7:c.*821C>T
|
ENSP00000420445.3:n.*821C>T
|
|
ENST00000491243.5:n.1582C>T
|
|
|
ENST00000537758.5:c.1171C>T
|
ENSP00000446401.2:p.Arg391Ter
|
|
ENST00000537758.6:c.1153C>T
|
ENSP00000446401.3:p.Arg385Ter
|
|
ENST00000682661.1:n.2778C>T
|
|
|
ENST00000683804.1:n.1463C>T
|
|
|
ENST00000683923.1:c.1153C>T
|
ENSP00000506737.1:p.Arg385Ter
|
|
ENST00000684722.1:n.2740C>T
|
|
|
XM_005272635.1:c.1510C>T
|
XP_005272692.1:p.Arg504Ter
|
|
XM_005272636.1:c.1492C>T
|
XP_005272693.1:p.Arg498Ter
|
|
XM_005272637.1:c.1438C>T
|
XP_005272694.1:p.Arg480Ter
|
|
XM_006724544.2:c.1291C>T
|
XP_006724607.1:p.Arg431Ter
|
|
XM_006724545.2:c.1237C>T
|
XP_006724608.1:p.Arg413Ter
|
|
XM_006724546.2:c.1186C>T
|
XP_006724609.1:p.Arg396Ter
|
|
XM_006724547.1:c.973C>T
|
XP_006724610.1:p.Arg325Ter
|
|
XM_011543948.1:c.940C>T
|
XP_011542250.1:p.Arg314Ter
|
