ENST00000675785.2:c.996C>A
|
ENSP00000502019.1:p.His332Gln
|
|
ENST00000373477.9:c.1143C>A
MANE Select
|
ENSP00000362576.4:p.His381Gln
|
|
ENST00000674629.1:c.*691C>A
|
ENSP00000502470.1:n.*691C>A
|
|
ENST00000674654.1:c.*1103C>A
|
ENSP00000501729.1:n.*1103C>A
|
|
ENST00000675785.1:c.996C>A
|
ENSP00000502019.1:p.His332Gln
|
|
ENST00000676297.1:c.*1317C>A
|
ENSP00000501596.1:n.*1317C>A
|
|
ENST00000373477.8:c.1143C>A
|
ENSP00000362576.4:p.His381Gln
|
|
ENST00000469100.5:n.1059C>A
|
|
|
ENST00000478828.1:n.610C>A
|
|
|
ENST00000487404.5:n.1453C>A
|
|
|
ENST00000490826.1:n.436C>A
|
|
|
ENST00000616261.1:c.1142C>A
|
ENSP00000484192.1:p.Thr381Asn
|
|
NM_003680.3:c.1143C>A , LRG_273t1:c.1143C>A
|
NP_003671.1:p.His381Gln
|
|
XM_011542347.1:c.513C>A
|
XP_011540649.1:p.His171Gln
|
|
XM_011542348.1:c.513C>A
|
XP_011540650.1:p.His171Gln
|
|
XM_011542347.2:c.513C>A
|
XP_011540649.1:p.His171Gln
|
|
XM_017002651.2:c.513C>A
|
XP_016858140.1:p.His171Gln
|
|
NM_003680.4:c.1143C>A
MANE Select
|
NP_003671.1:p.His381Gln
|
|