ENST00000502274.2:c.1805T>G
|
|
|
ENST00000515425.6:c.1909T>G
MANE Select
|
ENSP00000423660.1:p.Phe637Val
|
|
ENST00000675793.1:c.*1193T>G
|
ENSP00000502039.1:n.*1193T>G
|
|
ENST00000676056.1:c.*1419T>G
|
ENSP00000501827.1:n.*1419T>G
|
|
ENST00000323829.9:c.*1297T>G
|
ENSP00000313025.5:n.*1297T>G
|
|
ENST00000504517.5:c.1439T>G
|
ENSP00000421779.1:n.1439T>G
|
|
ENST00000504690.5:c.1909T>G
|
ENSP00000425627.1:p.Phe637Val
|
|
ENST00000510779.1:c.959T>G
|
|
|
ENST00000511307.5:c.*1689T>G
|
ENSP00000421420.1:n.*1689T>G
|
|
ENST00000512049.5:c.1888T>G
|
ENSP00000421860.1:p.Phe630Val
|
|
ENST00000513604.5:c.*1297T>G
|
ENSP00000423111.1:n.*1297T>G
|
|
ENST00000515425.5:c.1909T>G
|
ENSP00000423660.1:p.Phe637Val
|
|
NM_024577.3:c.1909T>G , LRG_269t1:c.1909T>G
|
NP_078853.2:p.Phe637Val
|
|
NM_024577.4:c.1909T>G
MANE Select
|
NP_078853.2:p.Phe637Val
|
|