ENST00000502274.2:c.3292G>T
|
|
|
ENST00000515425.6:c.3396G>T
MANE Select
|
ENSP00000423660.1:p.Leu1132=
|
|
ENST00000675793.1:c.*2680G>T
|
ENSP00000502039.1:n.*2680G>T
|
|
ENST00000323829.9:c.*2784G>T
|
ENSP00000313025.5:n.*2784G>T
|
|
ENST00000504517.5:c.2926G>T
|
ENSP00000421779.1:n.2926G>T
|
|
ENST00000504690.5:c.3396G>T
|
ENSP00000425627.1:p.Leu1132=
|
|
ENST00000510779.1:c.2446G>T
|
|
|
ENST00000512049.5:c.3375G>T
|
ENSP00000421860.1:p.Leu1125=
|
|
ENST00000515229.5:n.58G>T
|
|
|
ENST00000515425.5:c.3396G>T
|
ENSP00000423660.1:p.Leu1132=
|
|
NM_024577.3:c.3396G>T , LRG_269t1:c.3396G>T
|
NP_078853.2:p.Leu1132=
|
|
NM_024577.4:c.3396G>T
MANE Select
|
NP_078853.2:p.Leu1132=
|
|