ENST00000232607.7:c.413T>A
MANE Select
|
ENSP00000232607.2:p.Val138Asp
|
|
ENST00000232607.6:c.413T>A
|
ENSP00000232607.2:p.Val138Asp
|
|
ENST00000460034.5:c.*157T>A
|
ENSP00000420409.1:n.*157T>A
|
|
ENST00000462091.5:c.*85T>A
|
ENSP00000417893.1:n.*85T>A
|
|
ENST00000467167.5:c.*311T>A
|
ENSP00000419618.1:n.*311T>A
|
|
ENST00000474588.5:c.311-245T>A
|
ENSP00000420348.1:n.311-245T>A
|
|
ENST00000479719.5:c.413T>A
|
ENSP00000420754.1:p.Val138Asp
|
|
ENST00000497791.5:c.*85T>A
|
ENSP00000419121.1:n.*85T>A
|
|
ENST00000498715.1:n.131T>A
|
|
|
NM_000373.3:c.413T>A
|
NP_000364.1:p.Val138Asp
|
|
NR_033434.1:n.365T>A
|
|
|
NR_033437.1:n.618T>A
|
|
|
XR_001740253.2:n.443T>A
|
|
|
NM_000373.4:c.413T>A
MANE Select
|
NP_000364.1:p.Val138Asp
|
|
NR_033434.2:n.279T>A
|
|
|
NR_033437.2:n.532T>A
|
|
|