ENST00000314251.8:c.576T>A
MANE Select
|
ENSP00000323568.3:p.His192Gln
|
|
ENST00000314251.7:c.576T>A
|
ENSP00000323568.3:p.His192Gln
|
|
ENST00000461867.1:c.57T>A
|
ENSP00000418888.1:p.His19Gln
|
|
ENST00000469787.1:c.*43T>A
|
ENSP00000417918.1:n.*43T>A
|
|
ENST00000471379.1:n.287T>A
|
|
|
ENST00000497642.5:c.*43T>A
|
ENSP00000418456.1:n.*43T>A
|
|
NM_000340.1:c.576T>A
|
NP_000331.1:p.His192Gln
|
|
NM_001278658.1:c.219T>A
|
NP_001265587.1:p.His73Gln
|
|
NM_001278659.1:c.57T>A
|
NP_001265588.1:p.His19Gln
|
|
XM_011513087.1:c.531T>A
|
XP_011511389.1:p.His177Gln
|
|
XM_011513088.1:c.357T>A
|
XP_011511390.1:p.His119Gln
|
|
XM_011513089.1:c.57T>A
|
XP_011511391.1:p.His19Gln
|
|
XM_011513087.2:c.531T>A
|
XP_011511389.1:p.His177Gln
|
|
XM_024453720.1:c.57T>A
|
XP_024309488.1:p.His19Gln
|
|
NM_000340.2:c.576T>A
MANE Select
|
NP_000331.1:p.His192Gln
|
|
NM_001278658.2:c.219T>A
|
NP_001265587.1:p.His73Gln
|
|
NM_001278659.2:c.57T>A
|
NP_001265588.1:p.His19Gln
|
|