ENST00000502274.2:c.2851G>T
|
|
|
ENST00000515425.6:c.2955G>T
MANE Select
|
ENSP00000423660.1:p.Glu985Asp
|
|
ENST00000675793.1:c.*2239G>T
|
ENSP00000502039.1:n.*2239G>T
|
|
ENST00000676056.1:c.*2465G>T
|
ENSP00000501827.1:n.*2465G>T
|
|
ENST00000323829.9:c.*2343G>T
|
ENSP00000313025.5:n.*2343G>T
|
|
ENST00000504517.5:c.2485G>T
|
ENSP00000421779.1:n.2485G>T
|
|
ENST00000504690.5:c.2955G>T
|
ENSP00000425627.1:p.Glu985Asp
|
|
ENST00000510779.1:c.2005G>T
|
|
|
ENST00000511307.5:c.*2842G>T
|
ENSP00000421420.1:n.*2842G>T
|
|
ENST00000512049.5:c.2934G>T
|
ENSP00000421860.1:p.Glu978Asp
|
|
ENST00000513604.5:c.*2450G>T
|
ENSP00000423111.1:n.*2450G>T
|
|
ENST00000515425.5:c.2955G>T
|
ENSP00000423660.1:p.Glu985Asp
|
|
NM_024577.3:c.2955G>T , LRG_269t1:c.2955G>T
|
NP_078853.2:p.Glu985Asp
|
|
NM_024577.4:c.2955G>T
MANE Select
|
NP_078853.2:p.Glu985Asp
|
|