ENST00000426263.10:c.876T>A
MANE Select
|
ENSP00000416293.2:p.Tyr292Ter
|
|
ENST00000674545.1:n.194T>A
|
|
|
ENST00000674765.1:c.876T>A
|
ENSP00000501811.1:p.Tyr292Ter
|
|
ENST00000675112.1:n.1177T>A
|
|
|
ENST00000676254.1:n.1325T>A
|
|
|
ENST00000426263.7:c.876T>A
|
ENSP00000416293.2:p.Tyr292Ter
|
|
ENST00000439722.2:c.755T>A
|
ENSP00000395521.2:n.755T>A
|
|
ENST00000475162.3:c.415+1320T>A
|
|
|
ENST00000630287.2:c.*191T>A
|
ENSP00000486694.1:n.*191T>A
|
|
NM_006516.2:c.876T>A
|
NP_006507.2:p.Tyr292Ter
|
|
NM_006516.3:c.876T>A
|
NP_006507.2:p.Tyr292Ter
|
|
NM_006516.4:c.876T>A
MANE Select
|
NP_006507.2:p.Tyr292Ter
|
|