ENST00000502274.2:c.1602C>T
|
|
|
ENST00000515425.6:c.1706C>T
MANE Select
|
ENSP00000423660.1:p.Ala569Val
|
|
ENST00000675793.1:c.*990C>T
|
ENSP00000502039.1:n.*990C>T
|
|
ENST00000676056.1:c.*1216C>T
|
ENSP00000501827.1:n.*1216C>T
|
|
ENST00000323829.9:c.*1094C>T
|
ENSP00000313025.5:n.*1094C>T
|
|
ENST00000504517.5:c.1236C>T
|
ENSP00000421779.1:n.1236C>T
|
|
ENST00000504690.5:c.1706C>T
|
ENSP00000425627.1:p.Ala569Val
|
|
ENST00000510779.1:c.756C>T
|
|
|
ENST00000511307.5:c.*1486C>T
|
ENSP00000421420.1:n.*1486C>T
|
|
ENST00000512049.5:c.1685C>T
|
ENSP00000421860.1:p.Ala562Val
|
|
ENST00000513604.5:c.*1094C>T
|
ENSP00000423111.1:n.*1094C>T
|
|
ENST00000515425.5:c.1706C>T
|
ENSP00000423660.1:p.Ala569Val
|
|
NM_024577.3:c.1706C>T , LRG_269t1:c.1706C>T
|
NP_078853.2:p.Ala569Val
|
|
NM_024577.4:c.1706C>T
MANE Select
|
NP_078853.2:p.Ala569Val
|
|