|
ENST00000696231.1:c.575C>G
|
ENSP00000512497.1:p.Ala192Gly
|
|
|
ENST00000696232.1:c.575C>G
|
ENSP00000512498.1:p.Ala192Gly
|
|
|
ENST00000696233.1:c.575C>G
|
ENSP00000512499.1:p.Ala192Gly
|
|
|
ENST00000696234.1:n.559C>G
|
|
|
|
ENST00000696235.1:c.449C>G
|
ENSP00000512500.1:p.Ala150Gly
|
|
|
ENST00000696236.1:c.449C>G
|
ENSP00000512501.1:p.Ala150Gly
|
|
|
ENST00000696237.1:n.681C>G
|
|
|
|
ENST00000696238.1:c.575C>G
|
ENSP00000512502.1:p.Ala192Gly
|
|
|
ENST00000696239.1:c.575C>G
|
ENSP00000512503.1:p.Ala192Gly
|
|
|
ENST00000201963.3:c.611C>G
|
ENSP00000201963.3:p.Ala204Gly
|
|
|
ENST00000328111.6:c.575C>G
MANE Select
|
ENSP00000328547.2:p.Ala192Gly
|
|
|
ENST00000348286.6:c.575C>G
|
ENSP00000337764.2:p.Ala192Gly
|
|
|
ENST00000353855.6:c.575C>G
|
ENSP00000313397.4:p.Ala192Gly
|
|
|
ENST00000443239.7:c.449C>G
|
ENSP00000403169.2:p.Ala150Gly
|
|
|
ENST00000456297.6:c.347C>G
|
ENSP00000412305.1:p.Ala116Gly
|
|
|
NM_001207055.1:c.449C>G
|
NP_001193984.1:p.Ala150Gly
|
|
|
NM_001207056.1:c.347C>G
|
NP_001193985.1:p.Ala116Gly
|
|
|
NM_006892.3:c.575C>G , LRG_56t1:c.575C>G
|
NP_008823.1:p.Ala192Gly
|
|
|
NM_175848.1:c.575C>G
|
NP_787044.1:p.Ala192Gly
|
|
|
NM_175849.1:c.575C>G
|
NP_787045.1:p.Ala192Gly
|
|
|
NM_175850.2:c.611C>G
|
NP_787046.1:p.Ala204Gly
|
|
|
XM_011528653.1:c.611C>G
|
XP_011526955.1:p.Ala204Gly
|
|
|
XM_011528654.1:c.485C>G
|
XP_011526956.1:p.Ala162Gly
|
|
|
XR_936510.1:n.747C>G
|
|
|
|
XR_936511.1:n.747C>G
|
|
|
|
XR_936512.1:n.622C>G
|
|
|
|
XM_011528653.2:c.611C>G
|
XP_011526955.1:p.Ala204Gly
|
|
|
XM_011528654.2:c.485C>G
|
XP_011526956.1:p.Ala162Gly
|
|
|
XR_936510.2:n.758C>G
|
|
|
|
XR_936511.2:n.758C>G
|
|
|
|
XR_936512.2:n.634C>G
|
|
|
|
NM_001207055.2:c.449C>G
|
NP_001193984.1:p.Ala150Gly
|
|
|
NM_001207056.2:c.347C>G
|
NP_001193985.1:p.Ala116Gly
|
|
|
NM_006892.4:c.575C>G
MANE Select
|
NP_008823.1:p.Ala192Gly
|
|
|
NM_175848.2:c.575C>G
|
NP_787044.1:p.Ala192Gly
|
|
|
NM_175849.2:c.575C>G
|
NP_787045.1:p.Ala192Gly
|
|
|
NM_175850.3:c.611C>G
|
NP_787046.1:p.Ala204Gly
|
|
