ENST00000502274.2:c.4354G>C
|
|
|
ENST00000515425.6:c.3501G>C
MANE Select
|
ENSP00000423660.1:p.Val1167=
|
|
ENST00000675793.1:c.*4558G>C
|
ENSP00000502039.1:n.*4558G>C
|
|
ENST00000323829.9:c.*2889G>C
|
ENSP00000313025.5:n.*2889G>C
|
|
ENST00000502274.1:c.87G>C
|
ENSP00000421092.1:p.Val29=
|
|
ENST00000504517.5:c.3023G>C
|
ENSP00000421779.1:n.3023G>C
|
|
ENST00000504690.5:c.3501G>C
|
ENSP00000425627.1:p.Val1167=
|
|
ENST00000510350.1:n.57G>C
|
|
|
ENST00000510779.1:c.2551G>C
|
|
|
ENST00000512049.5:c.3480G>C
|
ENSP00000421860.1:p.Val1160=
|
|
ENST00000515229.5:n.163G>C
|
|
|
ENST00000515425.5:c.3501G>C
|
ENSP00000423660.1:p.Val1167=
|
|
NM_024577.3:c.3501G>C , LRG_269t1:c.3501G>C
|
NP_078853.2:p.Val1167=
|
|
NM_024577.4:c.3501G>C
MANE Select
|
NP_078853.2:p.Val1167=
|
|