ENST00000651671.1:c.6036G>T
MANE Select
|
ENSP00000498587.1:p.Glu2012Asp
|
|
ENST00000679595.1:c.*1076G>T
|
ENSP00000506241.1:n.*1076G>T
|
|
ENST00000679969.1:n.2517G>T
|
|
|
ENST00000680003.1:n.2368G>T
|
|
|
ENST00000680133.1:c.5922G>T
|
ENSP00000505319.1:p.Glu1974Asp
|
|
ENST00000680218.1:c.5916G>T
|
ENSP00000505339.1:p.Glu1972Asp
|
|
ENST00000680668.1:c.5922G>T
|
ENSP00000506336.1:p.Glu1974Asp
|
|
ENST00000680778.1:c.3633G>T
|
ENSP00000506033.1:p.Glu1211Asp
|
|
ENST00000680924.1:c.*3436G>T
|
ENSP00000506031.1:n.*3436G>T
|
|
ENST00000681135.1:c.*3645G>T
|
ENSP00000506636.1:n.*3645G>T
|
|
ENST00000681298.1:n.4141G>T
|
|
|
ENST00000681454.1:c.*5272G>T
|
ENSP00000505763.1:n.*5272G>T
|
|
ENST00000277541.6:c.6036G>T
|
ENSP00000277541.6:p.Glu2012Asp
|
|
NM_017617.3:c.6036G>T
|
NP_060087.3:p.Glu2012Asp
|
|
XM_011518717.1:c.5337G>T
|
XP_011517019.1:p.Glu1779Asp
|
|
NM_017617.5:c.6036G>T
MANE Select
|
NP_060087.3:p.Glu2012Asp
|
|
XM_011518717.2:c.5313G>T
|
XP_011517019.2:p.Glu1771Asp
|
|