ENST00000675785.2:c.1018G=
|
ENSP00000502019.1:p.Val340=
|
|
ENST00000373477.9:c.1165G=
MANE Select
|
ENSP00000362576.4:p.Val389=
|
|
ENST00000674629.1:c.*713G=
|
ENSP00000502470.1:n.*713G=
|
|
ENST00000674654.1:c.*1125G=
|
ENSP00000501729.1:n.*1125G=
|
|
ENST00000675785.1:c.1018G=
|
ENSP00000502019.1:p.Val340=
|
|
ENST00000676297.1:c.*1339G=
|
ENSP00000501596.1:n.*1339G=
|
|
ENST00000373477.8:c.1165G=
|
ENSP00000362576.4:p.Val389=
|
|
ENST00000469100.5:n.1081G=
|
|
|
ENST00000478828.1:n.632G=
|
|
|
ENST00000487404.5:n.1475G=
|
|
|
ENST00000490826.1:n.458G=
|
|
|
ENST00000616261.1:c.1164G=
|
ENSP00000484192.1:p.Met388=
|
|
NM_003680.3:c.1165G= , LRG_273t1:c.1165G=
|
NP_003671.1:p.Val389=
|
|
XM_011542347.1:c.535G=
|
XP_011540649.1:p.Val179=
|
|
XM_011542348.1:c.535G=
|
XP_011540650.1:p.Val179=
|
|
XM_011542347.2:c.535G=
|
XP_011540649.1:p.Val179=
|
|
XM_017002651.2:c.535G=
|
XP_016858140.1:p.Val179=
|
|
NM_003680.4:c.1165G=
MANE Select
|
NP_003671.1:p.Val389=
|
|