ENST00000368074.6:c.936C>T
MANE Select
|
ENSP00000357053.1:p.Asp312=
|
|
ENST00000556710.6:c.*1520C>T
|
ENSP00000451235.2:n.*1520C>T
|
|
ENST00000647676.1:c.1274C>T
|
ENSP00000497162.1:n.1274C>T
|
|
ENST00000326837.6:c.936C>T
|
ENSP00000318227.2:p.Asp312=
|
|
ENST00000368073.7:c.936C>T
|
ENSP00000357052.3:p.Asp312=
|
|
ENST00000368074.5:c.936C>T
|
ENSP00000357053.1:p.Asp312=
|
|
ENST00000461888.5:c.936C>T
|
ENSP00000476407.1:p.Asp312=
|
|
ENST00000466253.1:n.451C>T
|
|
|
ENST00000556710.5:c.1398C>T
|
ENSP00000451235.1:p.Asp466=
|
|
NM_015726.3:c.936C>T
|
NP_056541.2:p.Asp312=
|
|
NR_028103.1:n.1448C>T
|
|
|
NR_028104.1:n.1374C>T
|
|
|
NM_015726.4:c.936C>T
MANE Select
|
NP_056541.2:p.Asp312=
|
|
NR_028103.2:n.1469C>T
|
|
|
NR_028104.2:n.1395C>T
|
|
|