|
NM_203475.3:c.727C>T
MANE Select
|
NP_982301.1:p.Arg243Ter
|
|
ENST00000326194.11:c.727C>T
MANE Select
|
ENSP00000322304.6:p.Arg243Ter
|
|
NM_001282167.1:c.481C>T
|
NP_001269096.1:p.Arg161Ter
|
|
NM_001282167.2:c.481C>T
|
NP_001269096.1:p.Arg161Ter
|
|
NM_022825.3:c.694C>T
|
NP_073736.2:p.Arg232Ter
|
|
NM_022825.4:c.694C>T
|
NP_073736.2:p.Arg232Ter
|
|
NM_203473.2:c.712C>T
|
NP_982299.1:p.Arg238Ter
|
|
NM_203473.3:c.712C>T
|
NP_982299.1:p.Arg238Ter
|
|
NM_203474.1:c.709C>T
|
NP_982300.1:p.Arg237Ter
|
|
NM_203475.2:c.727C>T
|
NP_982301.1:p.Arg243Ter
|
|
ENST00000326194.10:c.727C>T
|
ENSP00000322304.6:p.Arg243Ter
|
|
ENST00000355092.4:c.559C>T
|
ENSP00000347207.4:p.Arg187Ter
|
|
ENST00000355961.8:c.712C>T
|
ENSP00000348233.4:p.Arg238Ter
|
|
ENST00000359882.8:c.709C>T
|
ENSP00000352946.4:p.Arg237Ter
|
|
ENST00000361988.7:c.694C>T
|
ENSP00000354978.3:p.Arg232Ter
|
|
ENST00000367574.8:c.709C>T
|
ENSP00000356546.5:p.Arg237Ter
|
|
ENST00000367574.9:c.694C>T
|
ENSP00000356546.6:p.Arg232Ter
|
|
ENST00000472520.5:c.*35C>T
|
ENSP00000419858.1:n.*35C>T
|
|
ENST00000485288.6:c.*362C>T
|
ENSP00000420445.2:n.*362C>T
|
|
ENST00000485288.7:c.*362C>T
|
ENSP00000420445.3:n.*362C>T
|
|
ENST00000491243.5:n.1123C>T
|
|
|
ENST00000537758.5:c.712C>T
|
ENSP00000446401.2:p.Arg238Ter
|
|
ENST00000537758.6:c.694C>T
|
ENSP00000446401.3:p.Arg232Ter
|
|
ENST00000682661.1:n.2160C>T
|
|
|
ENST00000683923.1:c.694C>T
|
ENSP00000506737.1:p.Arg232Ter
|
|
ENST00000684722.1:n.2281C>T
|
|
|
XM_005272635.1:c.1051C>T
|
XP_005272692.1:p.Arg351Ter
|
|
XM_005272636.1:c.1033C>T
|
XP_005272693.1:p.Arg345Ter
|
|
XM_005272637.1:c.979C>T
|
XP_005272694.1:p.Arg327Ter
|
|
XM_006724544.2:c.832C>T
|
XP_006724607.1:p.Arg278Ter
|
|
XM_006724545.2:c.778C>T
|
XP_006724608.1:p.Arg260Ter
|
|
XM_006724546.2:c.727C>T
|
XP_006724609.1:p.Arg243Ter
|
|
XM_006724547.1:c.514C>T
|
XP_006724610.1:p.Arg172Ter
|
|
XM_011543948.1:c.481C>T
|
XP_011542250.1:p.Arg161Ter
|
|
XM_024452425.1:c.1066C>T
|
XP_024308193.1:p.Arg356Ter
|
