|
NM_004082.5:c.3145C>T
MANE Select
|
NP_004073.2:p.Arg1049Trp
|
|
ENST00000628224.3:c.3145C>T
MANE Select
|
ENSP00000487279.2:p.Arg1049Trp
|
|
NM_001135040.2:c.3085C>T
|
NP_001128512.1:p.Arg1029Trp
|
|
NM_001135040.3:c.3085C>T
|
NP_001128512.1:p.Arg1029Trp
|
|
NM_001135041.2:c.2743C>T
|
NP_001128513.1:p.Arg915Trp
|
|
NM_001135041.3:c.2743C>T
|
NP_001128513.1:p.Arg915Trp
|
|
NM_001190836.1:c.3034C>T
|
NP_001177765.1:p.Arg1012Trp
|
|
NM_001190836.2:c.3034C>T
|
NP_001177765.1:p.Arg1012Trp
|
|
NM_001190837.1:c.3124C>T
|
NP_001177766.1:p.Arg1042Trp
|
|
NM_001190837.2:c.3124C>T
|
NP_001177766.1:p.Arg1042Trp
|
|
NM_001378991.1:c.3094C>T
|
NP_001365920.1:p.Arg1032Trp
|
|
NM_001378992.1:c.3076C>T
|
NP_001365921.1:p.Arg1026Trp
|
|
NM_004082.4:c.3145C>T
|
NP_004073.2:p.Arg1049Trp
|
|
NM_023019.3:c.2743C>T
|
NP_075408.1:p.Arg915Trp
|
|
NM_023019.4:c.2743C>T
|
NP_075408.1:p.Arg915Trp
|
|
NR_033935.1:n.3429C>T
|
|
|
NR_033935.2:n.3208C>T
|
|
|
ENST00000361874.7:c.3145C>T
|
ENSP00000354791.3:p.Arg1049Trp
|
|
ENST00000361874.8:c.3145C>T
|
ENSP00000354791.4:p.Arg1049Trp
|
|
ENST00000394003.7:c.3124C>T
|
ENSP00000377571.3:p.Arg1042Trp
|
|
ENST00000409240.5:c.3034C>T
|
ENSP00000386406.1:p.Arg1012Trp
|
|
ENST00000409438.5:c.2743C>T
|
ENSP00000387270.1:p.Arg915Trp
|
|
ENST00000409567.7:c.3085C>T
|
ENSP00000386843.3:p.Arg1029Trp
|
|
ENST00000409868.5:c.3094C>T
|
ENSP00000387327.1:p.Arg1032Trp
|
|
ENST00000434055.5:c.*444C>T
|
ENSP00000416711.1:n.*444C>T
|
|
ENST00000466110.5:n.4397C>T
|
|
|
ENST00000497666.1:n.97-3589C>T
|
|
|
ENST00000628224.2:c.3094C>T
|
ENSP00000487279.1:p.Arg1032Trp
|
|
ENST00000633691.1:c.2743C>T
|
ENSP00000487724.1:p.Arg915Trp
|
|
ENST00000680606.1:c.3094C>T
|
ENSP00000505612.1:p.Arg1032Trp
|
