ENST00000426263.10:c.781G>T
MANE Select
|
ENSP00000416293.2:p.Glu261Ter
|
|
ENST00000669445.1:c.111G>T
|
|
|
ENST00000674765.1:c.781G>T
|
ENSP00000501811.1:p.Glu261Ter
|
|
ENST00000675112.1:n.804G>T
|
|
|
ENST00000676254.1:n.1230G>T
|
|
|
ENST00000426263.7:c.781G>T
|
ENSP00000416293.2:p.Glu261Ter
|
|
ENST00000439722.2:c.660G>T
|
ENSP00000395521.2:n.660G>T
|
|
ENST00000475162.3:c.415+947G>T
|
|
|
ENST00000630287.2:c.*96G>T
|
ENSP00000486694.1:n.*96G>T
|
|
NM_006516.2:c.781G>T
|
NP_006507.2:p.Glu261Ter
|
|
NM_006516.3:c.781G>T
|
NP_006507.2:p.Glu261Ter
|
|
NM_006516.4:c.781G>T
MANE Select
|
NP_006507.2:p.Glu261Ter
|
|