ENST00000502274.2:c.2038C>T
|
|
|
ENST00000515425.6:c.2142C>T
MANE Select
|
ENSP00000423660.1:p.Val714=
|
|
ENST00000675793.1:c.*1426C>T
|
ENSP00000502039.1:n.*1426C>T
|
|
ENST00000676056.1:c.*1652C>T
|
ENSP00000501827.1:n.*1652C>T
|
|
ENST00000323829.9:c.*1530C>T
|
ENSP00000313025.5:n.*1530C>T
|
|
ENST00000504517.5:c.1672C>T
|
ENSP00000421779.1:n.1672C>T
|
|
ENST00000504690.5:c.2142C>T
|
ENSP00000425627.1:p.Val714=
|
|
ENST00000510779.1:c.1192C>T
|
|
|
ENST00000511307.5:c.*1922C>T
|
ENSP00000421420.1:n.*1922C>T
|
|
ENST00000512049.5:c.2121C>T
|
ENSP00000421860.1:p.Val707=
|
|
ENST00000513604.5:c.*1530C>T
|
ENSP00000423111.1:n.*1530C>T
|
|
ENST00000515425.5:c.2142C>T
|
ENSP00000423660.1:p.Val714=
|
|
NM_024577.3:c.2142C>T , LRG_269t1:c.2142C>T
|
NP_078853.2:p.Val714=
|
|
NM_024577.4:c.2142C>T
MANE Select
|
NP_078853.2:p.Val714=
|
|