ENST00000690565.1:c.1456A>T
|
ENSP00000510501.1:p.Arg486Trp
|
|
ENST00000691308.1:c.829-153A>T
|
ENSP00000509583.1:n.829-153A>T
|
|
ENST00000448666.7:c.1456A>T
MANE Select
|
ENSP00000410992.3:p.Arg486Trp
|
|
ENST00000452063.7:c.1138A>T
|
ENSP00000388201.2:p.Arg380Trp
|
|
ENST00000462443.2:c.631A>T
|
ENSP00000497265.1:p.Arg211Trp
|
|
ENST00000647723.1:c.1399A>T
|
|
|
ENST00000647753.1:c.*749A>T
|
ENSP00000497318.1:n.*749A>T
|
|
ENST00000647771.1:c.*944A>T
|
ENSP00000496788.1:n.*944A>T
|
|
ENST00000647915.1:c.*749A>T
|
ENSP00000498123.1:n.*749A>T
|
|
ENST00000648768.1:n.1713A>T
|
|
|
ENST00000648810.1:c.631A>T
|
ENSP00000496949.1:p.Arg211Trp
|
|
ENST00000649075.1:c.*384A>T
|
ENSP00000497836.1:n.*384A>T
|
|
ENST00000649601.1:c.*636A>T
|
ENSP00000496796.1:n.*636A>T
|
|
ENST00000649777.1:n.1665A>T
|
|
|
ENST00000649854.1:c.1089A>T
|
|
|
ENST00000650523.1:c.1231A>T
|
ENSP00000497143.1:p.Arg411Trp
|
|
ENST00000233616.8:c.1456A>T
|
ENSP00000233616.4:p.Arg486Trp
|
|
ENST00000409065.5:c.*636A>T
|
ENSP00000386493.1:n.*636A>T
|
|
ENST00000448666.5:c.1138A>T
|
ENSP00000410992.1:p.Arg380Trp
|
|
ENST00000452063.6:c.1138A>T
|
ENSP00000388201.2:p.Arg380Trp
|
|
ENST00000462189.1:n.1137A>T
|
|
|
NM_001146158.1:c.1138A>T
|
NP_001139630.1:p.Arg380Trp
|
|
NM_006302.2:c.1456A>T
|
NP_006293.2:p.Arg486Trp
|
|
NM_006302.3:c.1456A>T
MANE Select
|
NP_006293.2:p.Arg486Trp
|
|
NM_001146158.2:c.1138A>T
|
NP_001139630.1:p.Arg380Trp
|
|