ENST00000696170.1:c.*408T>A
|
ENSP00000512461.1:n.*408T>A
|
|
ENST00000696171.1:c.803T>A
|
ENSP00000512462.1:p.Val268Glu
|
|
ENST00000378588.5:c.899T>A
MANE Select
|
ENSP00000367851.4:p.Val300Glu
|
|
ENST00000378588.4:c.899T>A
|
ENSP00000367851.4:p.Val300Glu
|
|
ENST00000465127.1:c.171+377878T>A
|
ENSP00000417050.1:n.171+377878T>A
|
|
ENST00000492288.1:n.324T>A
|
|
|
NM_000397.3:c.899T>A , LRG_53t1:c.899T>A
|
NP_000388.2:p.Val300Glu
|
|
XM_011543890.1:c.593T>A
|
XP_011542192.1:p.Val198Glu
|
|
NM_000397.4:c.899T>A
MANE Select
|
NP_000388.2:p.Val300Glu
|
|