ENST00000675785.2:c.1006G>T
|
ENSP00000502019.1:p.Asp336Tyr
|
|
ENST00000373477.9:c.1153G>T
MANE Select
|
ENSP00000362576.4:p.Asp385Tyr
|
|
ENST00000674629.1:c.*701G>T
|
ENSP00000502470.1:n.*701G>T
|
|
ENST00000674654.1:c.*1113G>T
|
ENSP00000501729.1:n.*1113G>T
|
|
ENST00000675785.1:c.1006G>T
|
ENSP00000502019.1:p.Asp336Tyr
|
|
ENST00000676297.1:c.*1327G>T
|
ENSP00000501596.1:n.*1327G>T
|
|
ENST00000373477.8:c.1153G>T
|
ENSP00000362576.4:p.Asp385Tyr
|
|
ENST00000469100.5:n.1069G>T
|
|
|
ENST00000478828.1:n.620G>T
|
|
|
ENST00000487404.5:n.1463G>T
|
|
|
ENST00000490826.1:n.446G>T
|
|
|
ENST00000616261.1:c.1152G>T
|
ENSP00000484192.1:p.Gln384His
|
|
NM_003680.3:c.1153G>T , LRG_273t1:c.1153G>T
|
NP_003671.1:p.Asp385Tyr
|
|
XM_011542347.1:c.523G>T
|
XP_011540649.1:p.Asp175Tyr
|
|
XM_011542348.1:c.523G>T
|
XP_011540650.1:p.Asp175Tyr
|
|
XM_011542347.2:c.523G>T
|
XP_011540649.1:p.Asp175Tyr
|
|
XM_017002651.2:c.523G>T
|
XP_016858140.1:p.Asp175Tyr
|
|
NM_003680.4:c.1153G>T
MANE Select
|
NP_003671.1:p.Asp385Tyr
|
|