ENST00000675785.2:c.1158G>C
|
ENSP00000502019.1:p.Glu386Asp
|
|
ENST00000373477.9:c.1305G>C
MANE Select
|
ENSP00000362576.4:p.Glu435Asp
|
|
ENST00000674629.1:c.*853G>C
|
ENSP00000502470.1:n.*853G>C
|
|
ENST00000674654.1:c.*1265G>C
|
ENSP00000501729.1:n.*1265G>C
|
|
ENST00000675785.1:c.1158G>C
|
ENSP00000502019.1:p.Glu386Asp
|
|
ENST00000676297.1:c.*1479G>C
|
ENSP00000501596.1:n.*1479G>C
|
|
ENST00000373477.8:c.1305G>C
|
ENSP00000362576.4:p.Glu435Asp
|
|
ENST00000469100.5:n.1221G>C
|
|
|
ENST00000478828.1:n.772G>C
|
|
|
ENST00000487404.5:n.1615G>C
|
|
|
ENST00000490826.1:n.598G>C
|
|
|
NM_003680.3:c.1305G>C , LRG_273t1:c.1305G>C
|
NP_003671.1:p.Glu435Asp
|
|
XM_011542347.1:c.675G>C
|
XP_011540649.1:p.Glu225Asp
|
|
XM_011542348.1:c.675G>C
|
XP_011540650.1:p.Glu225Asp
|
|
XM_011542347.2:c.675G>C
|
XP_011540649.1:p.Glu225Asp
|
|
XM_017002651.2:c.675G>C
|
XP_016858140.1:p.Glu225Asp
|
|
NM_003680.4:c.1305G>C
MANE Select
|
NP_003671.1:p.Glu435Asp
|
|