ENST00000675785.2:c.1040A>T
|
ENSP00000502019.1:p.Glu347Val
|
|
ENST00000373477.9:c.1187A>T
MANE Select
|
ENSP00000362576.4:p.Glu396Val
|
|
ENST00000674629.1:c.*735A>T
|
ENSP00000502470.1:n.*735A>T
|
|
ENST00000674654.1:c.*1147A>T
|
ENSP00000501729.1:n.*1147A>T
|
|
ENST00000675785.1:c.1040A>T
|
ENSP00000502019.1:p.Glu347Val
|
|
ENST00000676297.1:c.*1361A>T
|
ENSP00000501596.1:n.*1361A>T
|
|
ENST00000373477.8:c.1187A>T
|
ENSP00000362576.4:p.Glu396Val
|
|
ENST00000469100.5:n.1103A>T
|
|
|
ENST00000478828.1:n.654A>T
|
|
|
ENST00000487404.5:n.1497A>T
|
|
|
ENST00000490826.1:n.480A>T
|
|
|
NM_003680.3:c.1187A>T , LRG_273t1:c.1187A>T
|
NP_003671.1:p.Glu396Val
|
|
XM_011542347.1:c.557A>T
|
XP_011540649.1:p.Glu186Val
|
|
XM_011542348.1:c.557A>T
|
XP_011540650.1:p.Glu186Val
|
|
XM_011542347.2:c.557A>T
|
XP_011540649.1:p.Glu186Val
|
|
XM_017002651.2:c.557A>T
|
XP_016858140.1:p.Glu186Val
|
|
NM_003680.4:c.1187A>T
MANE Select
|
NP_003671.1:p.Glu396Val
|
|