ENST00000502274.2:c.1707A>T
|
|
|
ENST00000515425.6:c.1811A>T
MANE Select
|
ENSP00000423660.1:p.Asp604Val
|
|
ENST00000675793.1:c.*1095A>T
|
ENSP00000502039.1:n.*1095A>T
|
|
ENST00000676056.1:c.*1321A>T
|
ENSP00000501827.1:n.*1321A>T
|
|
ENST00000323829.9:c.*1199A>T
|
ENSP00000313025.5:n.*1199A>T
|
|
ENST00000504517.5:c.1341A>T
|
ENSP00000421779.1:n.1341A>T
|
|
ENST00000504690.5:c.1811A>T
|
ENSP00000425627.1:p.Asp604Val
|
|
ENST00000510779.1:c.861A>T
|
|
|
ENST00000511307.5:c.*1591A>T
|
ENSP00000421420.1:n.*1591A>T
|
|
ENST00000512049.5:c.1790A>T
|
ENSP00000421860.1:p.Asp597Val
|
|
ENST00000513604.5:c.*1199A>T
|
ENSP00000423111.1:n.*1199A>T
|
|
ENST00000515425.5:c.1811A>T
|
ENSP00000423660.1:p.Asp604Val
|
|
NM_024577.3:c.1811A>T , LRG_269t1:c.1811A>T
|
NP_078853.2:p.Asp604Val
|
|
NM_024577.4:c.1811A>T
MANE Select
|
NP_078853.2:p.Asp604Val
|
|