ENST00000675785.2:c.1076A>G
|
ENSP00000502019.1:p.Gln359Arg
|
|
ENST00000373477.9:c.1223A>G
MANE Select
|
ENSP00000362576.4:p.Gln408Arg
|
|
ENST00000674629.1:c.*771A>G
|
ENSP00000502470.1:n.*771A>G
|
|
ENST00000674654.1:c.*1183A>G
|
ENSP00000501729.1:n.*1183A>G
|
|
ENST00000675785.1:c.1076A>G
|
ENSP00000502019.1:p.Gln359Arg
|
|
ENST00000676297.1:c.*1397A>G
|
ENSP00000501596.1:n.*1397A>G
|
|
ENST00000373477.8:c.1223A>G
|
ENSP00000362576.4:p.Gln408Arg
|
|
ENST00000469100.5:n.1139A>G
|
|
|
ENST00000478828.1:n.690A>G
|
|
|
ENST00000487404.5:n.1533A>G
|
|
|
ENST00000490826.1:n.516A>G
|
|
|
NM_003680.3:c.1223A>G , LRG_273t1:c.1223A>G
|
NP_003671.1:p.Gln408Arg
|
|
XM_011542347.1:c.593A>G
|
XP_011540649.1:p.Gln198Arg
|
|
XM_011542348.1:c.593A>G
|
XP_011540650.1:p.Gln198Arg
|
|
XM_011542347.2:c.593A>G
|
XP_011540649.1:p.Gln198Arg
|
|
XM_017002651.2:c.593A>G
|
XP_016858140.1:p.Gln198Arg
|
|
NM_003680.4:c.1223A>G
MANE Select
|
NP_003671.1:p.Gln408Arg
|
|