ENST00000350051.8:c.429A>G
MANE Select
|
ENSP00000324180.4:p.Ter143Trp
|
|
ENST00000301633.8:c.498A>G
|
ENSP00000301633.3:p.Ter166Trp
|
|
ENST00000350051.7:c.429A>G
|
ENSP00000324180.4:p.Ter143Trp
|
|
ENST00000374948.6:c.311A>G
|
ENSP00000364086.1:p.Glu104Gly
|
|
ENST00000589892.1:n.445A>G
|
|
|
ENST00000590925.6:c.*231A>G
|
ENSP00000467336.1:n.*231A>G
|
|
NM_001012270.1:c.311A>G
|
NP_001012270.1:p.Glu104Gly
|
|
NM_001012271.1:c.498A>G
|
NP_001012271.1:p.Ter166Trp
|
|
NM_001168.2:c.429A>G
|
NP_001159.2:p.Ter143Trp
|
|
XR_243654.3:n.631A>G
|
|
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XR_934452.1:n.700A>G
|
|
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XR_243654.5:n.631A>G
|
|
|
XR_934452.3:n.700A>G
|
|
|
NM_001168.3:c.429A>G
MANE Select
|
NP_001159.2:p.Ter143Trp
|
|
NM_001012270.2:c.311A>G
|
NP_001012270.1:p.Glu104Gly
|
|
NM_001012271.2:c.498A>G
|
NP_001012271.1:p.Ter166Trp
|
|