ENST00000675785.2:c.1015T>G
|
ENSP00000502019.1:p.Tyr339Asp
|
|
ENST00000373477.9:c.1162T>G
MANE Select
|
ENSP00000362576.4:p.Tyr388Asp
|
|
ENST00000674629.1:c.*710T>G
|
ENSP00000502470.1:n.*710T>G
|
|
ENST00000674654.1:c.*1122T>G
|
ENSP00000501729.1:n.*1122T>G
|
|
ENST00000675785.1:c.1015T>G
|
ENSP00000502019.1:p.Tyr339Asp
|
|
ENST00000676297.1:c.*1336T>G
|
ENSP00000501596.1:n.*1336T>G
|
|
ENST00000373477.8:c.1162T>G
|
ENSP00000362576.4:p.Tyr388Asp
|
|
ENST00000469100.5:n.1078T>G
|
|
|
ENST00000478828.1:n.629T>G
|
|
|
ENST00000487404.5:n.1472T>G
|
|
|
ENST00000490826.1:n.455T>G
|
|
|
ENST00000616261.1:c.1161T>G
|
ENSP00000484192.1:p.Cys387Trp
|
|
NM_003680.3:c.1162T>G , LRG_273t1:c.1162T>G
|
NP_003671.1:p.Tyr388Asp
|
|
XM_011542347.1:c.532T>G
|
XP_011540649.1:p.Tyr178Asp
|
|
XM_011542348.1:c.532T>G
|
XP_011540650.1:p.Tyr178Asp
|
|
XM_011542347.2:c.532T>G
|
XP_011540649.1:p.Tyr178Asp
|
|
XM_017002651.2:c.532T>G
|
XP_016858140.1:p.Tyr178Asp
|
|
NM_003680.4:c.1162T>G
MANE Select
|
NP_003671.1:p.Tyr388Asp
|
|