ENST00000675785.2:c.1051C>G
|
ENSP00000502019.1:p.Arg351Gly
|
|
ENST00000373477.9:c.1198C>G
MANE Select
|
ENSP00000362576.4:p.Arg400Gly
|
|
ENST00000674629.1:c.*746C>G
|
ENSP00000502470.1:n.*746C>G
|
|
ENST00000674654.1:c.*1158C>G
|
ENSP00000501729.1:n.*1158C>G
|
|
ENST00000675785.1:c.1051C>G
|
ENSP00000502019.1:p.Arg351Gly
|
|
ENST00000676297.1:c.*1372C>G
|
ENSP00000501596.1:n.*1372C>G
|
|
ENST00000373477.8:c.1198C>G
|
ENSP00000362576.4:p.Arg400Gly
|
|
ENST00000469100.5:n.1114C>G
|
|
|
ENST00000478828.1:n.665C>G
|
|
|
ENST00000487404.5:n.1508C>G
|
|
|
ENST00000490826.1:n.491C>G
|
|
|
NM_003680.3:c.1198C>G , LRG_273t1:c.1198C>G
|
NP_003671.1:p.Arg400Gly
|
|
XM_011542347.1:c.568C>G
|
XP_011540649.1:p.Arg190Gly
|
|
XM_011542348.1:c.568C>G
|
XP_011540650.1:p.Arg190Gly
|
|
XM_011542347.2:c.568C>G
|
XP_011540649.1:p.Arg190Gly
|
|
XM_017002651.2:c.568C>G
|
XP_016858140.1:p.Arg190Gly
|
|
NM_003680.4:c.1198C>G
MANE Select
|
NP_003671.1:p.Arg400Gly
|
|