ENST00000700100.1:c.665T>G
|
ENSP00000514797.1:p.Met222Arg
|
|
ENST00000700101.1:c.665T>G
|
ENSP00000514798.1:p.Met222Arg
|
|
ENST00000700102.1:n.2268T>G
|
|
|
ENST00000700103.1:n.3630T>G
|
|
|
ENST00000700104.1:c.*414T>G
|
ENSP00000514799.1:n.*414T>G
|
|
ENST00000308394.9:c.665T>G
MANE Select
|
ENSP00000311032.4:p.Met222Arg
|
|
ENST00000308394.8:c.665T>G
|
ENSP00000311032.4:p.Met222Arg
|
|
ENST00000393585.6:c.544T>G
|
ENSP00000377210.2:p.Cys182Gly
|
|
ENST00000393588.8:c.544T>G
|
ENSP00000377213.4:p.Cys182Gly
|
|
ENST00000517513.5:c.544T>G
|
ENSP00000428372.1:p.Cys182Gly
|
|
ENST00000523916.5:c.665T>G
|
ENSP00000428929.1:p.Met222Arg
|
|
ENST00000613118.4:c.*98T>G
|
ENSP00000478339.1:n.*98T>G
|
|
NM_004346.3:c.665T>G
|
NP_004337.2:p.Met222Arg
|
|
NM_032991.2:c.665T>G
|
NP_116786.1:p.Met222Arg
|
|
XM_011532301.1:c.665T>G
|
XP_011530603.1:p.Met222Arg
|
|
NM_001354777.1:c.665T>G
|
NP_001341706.1:p.Met222Arg
|
|
NM_001354779.1:c.587T>G
|
NP_001341708.1:p.Met196Arg
|
|
NM_001354780.1:c.587T>G
|
NP_001341709.1:p.Met196Arg
|
|
NM_001354781.1:c.544T>G
|
NP_001341710.1:p.Cys182Gly
|
|
NM_001354782.1:c.544T>G
|
NP_001341711.1:p.Cys182Gly
|
|
NM_001354783.1:c.571T>G
|
NP_001341712.1:p.Cys191Gly
|
|
NM_001354784.1:c.466T>G
|
NP_001341713.1:p.Cys156Gly
|
|
NM_004346.4:c.665T>G
MANE Select
|
NP_004337.2:p.Met222Arg
|
|
NM_001354777.2:c.665T>G
|
NP_001341706.1:p.Met222Arg
|
|
NM_001354779.2:c.587T>G
|
NP_001341708.1:p.Met196Arg
|
|
NM_001354780.2:c.587T>G
|
NP_001341709.1:p.Met196Arg
|
|
NM_001354781.2:c.544T>G
|
NP_001341710.1:p.Cys182Gly
|
|
NM_001354782.2:c.544T>G
|
NP_001341711.1:p.Cys182Gly
|
|
NM_001354783.2:c.571T>G
|
NP_001341712.1:p.Cys191Gly
|
|
NM_001354784.2:c.466T>G
|
NP_001341713.1:p.Cys156Gly
|
|
NM_032991.3:c.665T>G
|
NP_116786.1:p.Met222Arg
|
|