ENST00000383788.10:c.1075-27G>C
MANE Select
|
ENSP00000373298.3:n.1075-27G>C
|
|
ENST00000604401.2:n.931-27G>C
|
|
|
ENST00000679838.1:c.*837-27G>C
|
ENSP00000505708.1:n.*837-27G>C
|
|
ENST00000680240.1:n.987-27G>C
|
|
|
ENST00000680545.1:n.841-27G>C
|
|
|
ENST00000681097.1:c.*89-27G>C
|
ENSP00000505397.1:n.*89-27G>C
|
|
ENST00000681222.1:n.4566-27G>C
|
|
|
ENST00000383781.8:c.1045-27G>C
|
ENSP00000373291.3:n.1045-27G>C
|
|
ENST00000383786.9:c.973-27G>C
|
ENSP00000373296.3:n.973-27G>C
|
|
ENST00000383788.9:c.1075-27G>C
|
ENSP00000373298.3:n.1075-27G>C
|
|
ENST00000603808.5:c.1075-27G>C
|
ENSP00000474271.1:n.1075-27G>C
|
|
NM_005677.3:c.1075-27G>C
|
NP_005668.2:n.1075-27G>C
|
|
NM_080538.2:c.1045-27G>C
|
NP_536799.1:n.1045-27G>C
|
|
NM_080539.3:c.973-27G>C
|
NP_536800.2:n.973-27G>C
|
|
NM_005677.4:c.1075-27G>C
MANE Select
|
NP_005668.2:n.1075-27G>C
|
|
NM_080539.4:c.973-27G>C
|
NP_536800.2:n.973-27G>C
|
|