ENST00000696170.1:c.*523C>A
|
ENSP00000512461.1:n.*523C>A
|
|
ENST00000696171.1:c.918C>A
|
ENSP00000512462.1:p.His306Gln
|
|
ENST00000378588.5:c.1014C>A
MANE Select
|
ENSP00000367851.4:p.His338Gln
|
|
ENST00000378588.4:c.1014C>A
|
ENSP00000367851.4:p.His338Gln
|
|
ENST00000465127.1:c.171+377993C>A
|
ENSP00000417050.1:n.171+377993C>A
|
|
ENST00000492288.1:n.439C>A
|
|
|
NM_000397.3:c.1014C>A , LRG_53t1:c.1014C>A
|
NP_000388.2:p.His338Gln
|
|
XM_011543890.1:c.708C>A
|
XP_011542192.1:p.His236Gln
|
|
NM_000397.4:c.1014C>A
MANE Select
|
NP_000388.2:p.His338Gln
|
|