ENST00000706645.1:n.1586T>G
|
|
|
ENST00000281243.10:c.539T>G
MANE Select
|
ENSP00000281243.5:p.Val180Gly
|
|
ENST00000281243.9:c.539T>G
|
ENSP00000281243.5:p.Val180Gly
|
|
ENST00000428702.6:c.446T>G
|
ENSP00000390944.2:p.Val149Gly
|
|
ENST00000501943.6:n.276T>G
|
|
|
ENST00000505710.1:c.364-1493T>G
|
|
|
ENST00000507439.5:c.437-1493T>G
|
ENSP00000423227.1:n.437-1493T>G
|
|
ENST00000508623.5:c.437-5002T>G
|
ENSP00000426377.1:n.437-5002T>G
|
|
ENST00000511609.1:n.271T>G
|
|
|
ENST00000513615.5:c.437-1493T>G
|
ENSP00000422759.1:n.437-1493T>G
|
|
ENST00000514300.1:c.*368-1493T>G
|
ENSP00000426039.1:n.*368-1493T>G
|
|
NM_000320.2:c.539T>G
|
NP_000311.2:p.Val180Gly
|
|
NM_001306140.1:c.446T>G
|
NP_001293069.1:p.Val149Gly
|
|
XR_241677.1:n.600-1493T>G
|
|
|
NR_156494.1:n.617-1493T>G
|
|
|
NM_000320.3:c.539T>G
MANE Select
|
NP_000311.2:p.Val180Gly
|
|
NM_001306140.2:c.446T>G
|
NP_001293069.1:p.Val149Gly
|
|
NR_156494.2:n.473-1493T>G
|
|
|