ENST00000350051.8:c.373G>C
MANE Select
|
ENSP00000324180.4:p.Glu125Gln
|
|
ENST00000301633.8:c.442G>C
|
ENSP00000301633.3:p.Glu148Gln
|
|
ENST00000350051.7:c.373G>C
|
ENSP00000324180.4:p.Glu125Gln
|
|
ENST00000374948.6:c.255G>C
|
ENSP00000364086.1:p.Leu85Phe
|
|
ENST00000589892.1:n.389G>C
|
|
|
ENST00000590925.6:c.*175G>C
|
ENSP00000467336.1:n.*175G>C
|
|
NM_001012270.1:c.255G>C
|
NP_001012270.1:p.Leu85Phe
|
|
NM_001012271.1:c.442G>C
|
NP_001012271.1:p.Glu148Gln
|
|
NM_001168.2:c.373G>C
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NP_001159.2:p.Glu125Gln
|
|
XR_243654.3:n.575G>C
|
|
|
XR_934452.1:n.644G>C
|
|
|
XR_243654.5:n.575G>C
|
|
|
XR_934452.3:n.644G>C
|
|
|
NM_001168.3:c.373G>C
MANE Select
|
NP_001159.2:p.Glu125Gln
|
|
NM_001012270.2:c.255G>C
|
NP_001012270.1:p.Leu85Phe
|
|
NM_001012271.2:c.442G>C
|
NP_001012271.1:p.Glu148Gln
|
|