ENST00000502274.2:c.2895A=
|
|
|
ENST00000515425.6:c.2999A=
MANE Select
|
ENSP00000423660.1:p.Glu1000=
|
|
ENST00000675793.1:c.*2283A=
|
ENSP00000502039.1:n.*2283A=
|
|
ENST00000676056.1:c.*2509A=
|
ENSP00000501827.1:n.*2509A=
|
|
ENST00000323829.9:c.*2387A=
|
ENSP00000313025.5:n.*2387A=
|
|
ENST00000504517.5:c.2529A=
|
ENSP00000421779.1:n.2529A=
|
|
ENST00000504690.5:c.2999A=
|
ENSP00000425627.1:p.Glu1000=
|
|
ENST00000510779.1:c.2049A=
|
|
|
ENST00000511307.5:c.*2886A=
|
ENSP00000421420.1:n.*2886A=
|
|
ENST00000512049.5:c.2978A=
|
ENSP00000421860.1:p.Glu993=
|
|
ENST00000513604.5:c.*2494A=
|
ENSP00000423111.1:n.*2494A=
|
|
ENST00000515425.5:c.2999A=
|
ENSP00000423660.1:p.Glu1000=
|
|
NM_024577.3:c.2999A= , LRG_269t1:c.2999A=
|
NP_078853.2:p.Glu1000=
|
|
NM_024577.4:c.2999A=
MANE Select
|
NP_078853.2:p.Glu1000=
|
|