ENST00000502274.2:c.2890G>C
|
|
|
ENST00000515425.6:c.2994G>C
MANE Select
|
ENSP00000423660.1:p.Glu998Asp
|
|
ENST00000675793.1:c.*2278G>C
|
ENSP00000502039.1:n.*2278G>C
|
|
ENST00000676056.1:c.*2504G>C
|
ENSP00000501827.1:n.*2504G>C
|
|
ENST00000323829.9:c.*2382G>C
|
ENSP00000313025.5:n.*2382G>C
|
|
ENST00000504517.5:c.2524G>C
|
ENSP00000421779.1:n.2524G>C
|
|
ENST00000504690.5:c.2994G>C
|
ENSP00000425627.1:p.Glu998Asp
|
|
ENST00000510779.1:c.2044G>C
|
|
|
ENST00000511307.5:c.*2881G>C
|
ENSP00000421420.1:n.*2881G>C
|
|
ENST00000512049.5:c.2973G>C
|
ENSP00000421860.1:p.Glu991Asp
|
|
ENST00000513604.5:c.*2489G>C
|
ENSP00000423111.1:n.*2489G>C
|
|
ENST00000515425.5:c.2994G>C
|
ENSP00000423660.1:p.Glu998Asp
|
|
NM_024577.3:c.2994G>C , LRG_269t1:c.2994G>C
|
NP_078853.2:p.Glu998Asp
|
|
NM_024577.4:c.2994G>C
MANE Select
|
NP_078853.2:p.Glu998Asp
|
|