ENST00000368074.6:c.865-1G>T
MANE Select
|
ENSP00000357053.1:n.865-1G>T
|
|
ENST00000556710.6:c.*1449-1G>T
|
ENSP00000451235.2:n.*1449-1G>T
|
|
ENST00000647676.1:c.1203-1G>T
|
ENSP00000497162.1:n.1203-1G>T
|
|
ENST00000326837.6:c.865-1G>T
|
ENSP00000318227.2:n.865-1G>T
|
|
ENST00000368073.7:c.865-1G>T
|
ENSP00000357052.3:n.865-1G>T
|
|
ENST00000368074.5:c.865-1G>T
|
ENSP00000357053.1:n.865-1G>T
|
|
ENST00000461888.5:c.865-1G>T
|
ENSP00000476407.1:n.865-1G>T
|
|
ENST00000466253.1:n.380-1G>T
|
|
|
ENST00000556710.5:c.1327-1G>T
|
ENSP00000451235.1:n.1327-1G>T
|
|
NM_015726.3:c.865-1G>T
|
NP_056541.2:n.865-1G>T
|
|
NR_028103.1:n.1377-1G>T
|
|
|
NR_028104.1:n.1303-1G>T
|
|
|
NM_015726.4:c.865-1G>T
MANE Select
|
NP_056541.2:n.865-1G>T
|
|
NR_028103.2:n.1398-1G>T
|
|
|
NR_028104.2:n.1324-1G>T
|
|
|