ENST00000243964.7:c.2988A=
MANE Select
|
ENSP00000243964.4:p.Glu996=
|
|
ENST00000243964.6:c.2988A=
|
ENSP00000243964.3:p.Glu996=
|
|
ENST00000454036.6:c.3057A=
|
ENSP00000387694.1:p.Glu1019=
|
|
ENST00000616201.4:c.1298-2214A=
|
ENSP00000484585.1:n.1298-2214A=
|
|
ENST00000616202.4:c.613-2039A=
|
ENSP00000478369.1:n.613-2039A=
|
|
ENST00000616933.4:c.*2306A=
|
ENSP00000477569.1:n.*2306A=
|
|
ENST00000626937.2:c.510-3157A=
|
ENSP00000485953.1:n.510-3157A=
|
|
ENST00000628413.1:n.504A=
|
|
|
NM_001134771.1:c.3057A=
|
NP_001128243.1:p.Glu1019=
|
|
NM_020708.4:c.2988A=
|
NP_065759.1:p.Glu996=
|
|
XM_017027981.1:c.3057A=
|
XP_016883470.1:p.Glu1019=
|
|
NM_001134771.2:c.3057A=
|
NP_001128243.1:p.Glu1019=
|
|
NM_020708.5:c.2988A=
MANE Select
|
NP_065759.1:p.Glu996=
|
|