ENST00000696231.1:c.454G>T
|
ENSP00000512497.1:p.Ala152Ser
|
|
ENST00000696232.1:c.454G>T
|
ENSP00000512498.1:p.Ala152Ser
|
|
ENST00000696233.1:c.454G>T
|
ENSP00000512499.1:p.Ala152Ser
|
|
ENST00000696234.1:n.438G>T
|
|
|
ENST00000696235.1:c.328G>T
|
ENSP00000512500.1:p.Ala110Ser
|
|
ENST00000696236.1:c.328G>T
|
ENSP00000512501.1:p.Ala110Ser
|
|
ENST00000696237.1:n.560G>T
|
|
|
ENST00000696238.1:c.454G>T
|
ENSP00000512502.1:p.Ala152Ser
|
|
ENST00000696239.1:c.454G>T
|
ENSP00000512503.1:p.Ala152Ser
|
|
ENST00000201963.3:c.490G>T
|
ENSP00000201963.3:p.Ala164Ser
|
|
ENST00000328111.6:c.454G>T
MANE Select
|
ENSP00000328547.2:p.Ala152Ser
|
|
ENST00000348286.6:c.454G>T
|
ENSP00000337764.2:p.Ala152Ser
|
|
ENST00000353855.6:c.454G>T
|
ENSP00000313397.4:p.Ala152Ser
|
|
ENST00000443239.7:c.328G>T
|
ENSP00000403169.2:p.Ala110Ser
|
|
ENST00000456297.6:c.226G>T
|
ENSP00000412305.1:p.Ala76Ser
|
|
NM_001207055.1:c.328G>T
|
NP_001193984.1:p.Ala110Ser
|
|
NM_001207056.1:c.226G>T
|
NP_001193985.1:p.Ala76Ser
|
|
NM_006892.3:c.454G>T , LRG_56t1:c.454G>T
|
NP_008823.1:p.Ala152Ser
|
|
NM_175848.1:c.454G>T
|
NP_787044.1:p.Ala152Ser
|
|
NM_175849.1:c.454G>T
|
NP_787045.1:p.Ala152Ser
|
|
NM_175850.2:c.490G>T
|
NP_787046.1:p.Ala164Ser
|
|
XM_011528653.1:c.490G>T
|
XP_011526955.1:p.Ala164Ser
|
|
XM_011528654.1:c.364G>T
|
XP_011526956.1:p.Ala122Ser
|
|
XR_936510.1:n.626G>T
|
|
|
XR_936511.1:n.626G>T
|
|
|
XR_936512.1:n.501G>T
|
|
|
XM_011528653.2:c.490G>T
|
XP_011526955.1:p.Ala164Ser
|
|
XM_011528654.2:c.364G>T
|
XP_011526956.1:p.Ala122Ser
|
|
XR_936510.2:n.637G>T
|
|
|
XR_936511.2:n.637G>T
|
|
|
XR_936512.2:n.513G>T
|
|
|
NM_001207055.2:c.328G>T
|
NP_001193984.1:p.Ala110Ser
|
|
NM_001207056.2:c.226G>T
|
NP_001193985.1:p.Ala76Ser
|
|
NM_006892.4:c.454G>T
MANE Select
|
NP_008823.1:p.Ala152Ser
|
|
NM_175848.2:c.454G>T
|
NP_787044.1:p.Ala152Ser
|
|
NM_175849.2:c.454G>T
|
NP_787045.1:p.Ala152Ser
|
|
NM_175850.3:c.490G>T
|
NP_787046.1:p.Ala164Ser
|
|