|
NM_004082.5:c.3823C>T
MANE Select
|
NP_004073.2:p.Arg1275Cys
|
|
ENST00000628224.3:c.3823C>T
MANE Select
|
ENSP00000487279.2:p.Arg1275Cys
|
|
NM_001135040.2:c.3748C>T
|
NP_001128512.1:p.Arg1250Cys
|
|
NM_001135040.3:c.3748C>T
|
NP_001128512.1:p.Arg1250Cys
|
|
NM_001135041.2:c.3406C>T
|
NP_001128513.1:p.Arg1136Cys
|
|
NM_001135041.3:c.3406C>T
|
NP_001128513.1:p.Arg1136Cys
|
|
NM_001190836.1:c.3697C>T
|
NP_001177765.1:p.Arg1233Cys
|
|
NM_001190836.2:c.3697C>T
|
NP_001177765.1:p.Arg1233Cys
|
|
NM_001190837.1:c.3802C>T
|
NP_001177766.1:p.Arg1268Cys
|
|
NM_001190837.2:c.3802C>T
|
NP_001177766.1:p.Arg1268Cys
|
|
NM_001378991.1:c.3772C>T
|
NP_001365920.1:p.Arg1258Cys
|
|
NM_001378992.1:c.3754C>T
|
NP_001365921.1:p.Arg1252Cys
|
|
NM_004082.4:c.3823C>T
|
NP_004073.2:p.Arg1275Cys
|
|
NM_023019.3:c.3421C>T
|
NP_075408.1:p.Arg1141Cys
|
|
NM_023019.4:c.3421C>T
|
NP_075408.1:p.Arg1141Cys
|
|
NR_033935.1:n.4092C>T
|
|
|
NR_033935.2:n.3871C>T
|
|
|
ENST00000361874.7:c.3823C>T
|
ENSP00000354791.3:p.Arg1275Cys
|
|
ENST00000361874.8:c.3808C>T
|
ENSP00000354791.4:p.Arg1270Cys
|
|
ENST00000394003.7:c.3802C>T
|
ENSP00000377571.3:p.Arg1268Cys
|
|
ENST00000409240.5:c.3697C>T
|
ENSP00000386406.1:p.Arg1233Cys
|
|
ENST00000409438.5:c.3406C>T
|
ENSP00000387270.1:p.Arg1136Cys
|
|
ENST00000409567.7:c.3748C>T
|
ENSP00000386843.3:p.Arg1250Cys
|
|
ENST00000409868.5:c.3757C>T
|
ENSP00000387327.1:p.Arg1253Cys
|
|
ENST00000434055.5:c.*1107C>T
|
ENSP00000416711.1:n.*1107C>T
|
|
ENST00000451608.2:c.562C>T
|
ENSP00000416453.2:p.Arg188Cys
|
|
ENST00000466110.5:n.5060C>T
|
|
|
ENST00000491465.5:n.2086C>T
|
|
|
ENST00000497666.1:n.121C>T
|
|
|
ENST00000628224.2:c.3757C>T
|
ENSP00000487279.1:p.Arg1253Cys
|
|
ENST00000633691.1:c.3421C>T
|
ENSP00000487724.1:p.Arg1141Cys
|
|
ENST00000680606.1:c.3772C>T
|
ENSP00000505612.1:p.Arg1258Cys
|
