|
ENST00000696231.1:c.*770T>A
|
ENSP00000512497.1:n.*770T>A
|
|
|
ENST00000696232.1:c.1819T>A
|
ENSP00000512498.1:p.Cys607Ser
|
|
|
ENST00000696233.1:c.*562T>A
|
ENSP00000512499.1:n.*562T>A
|
|
|
ENST00000696235.1:c.*467T>A
|
ENSP00000512500.1:n.*467T>A
|
|
|
ENST00000696238.1:c.*562T>A
|
ENSP00000512502.1:n.*562T>A
|
|
|
ENST00000696239.1:c.1600T>A
|
ENSP00000512503.1:p.Cys534Ser
|
|
|
ENST00000201963.3:c.1795T>A
|
ENSP00000201963.3:p.Cys599Ser
|
|
|
ENST00000328111.6:c.1819T>A
MANE Select
|
ENSP00000328547.2:p.Cys607Ser
|
|
|
ENST00000348286.6:c.1759T>A
|
ENSP00000337764.2:p.Cys587Ser
|
|
|
ENST00000353855.6:c.1759T>A
|
ENSP00000313397.4:p.Cys587Ser
|
|
|
ENST00000443239.7:c.1633T>A
|
ENSP00000403169.2:p.Cys545Ser
|
|
|
ENST00000456297.6:c.1531T>A
|
ENSP00000412305.1:p.Cys511Ser
|
|
|
NM_001207055.1:c.1633T>A
|
NP_001193984.1:p.Cys545Ser
|
|
|
NM_001207056.1:c.1531T>A
|
NP_001193985.1:p.Cys511Ser
|
|
|
NM_006892.3:c.1819T>A , LRG_56t1:c.1819T>A
|
NP_008823.1:p.Cys607Ser
|
|
|
NM_175848.1:c.1759T>A
|
NP_787044.1:p.Cys587Ser
|
|
|
NM_175849.1:c.1759T>A
|
NP_787045.1:p.Cys587Ser
|
|
|
NM_175850.2:c.1795T>A
|
NP_787046.1:p.Cys599Ser
|
|
|
XM_011528653.1:c.1795T>A
|
XP_011526955.1:p.Cys599Ser
|
|
|
XM_011528654.1:c.1669T>A
|
XP_011526956.1:p.Cys557Ser
|
|
|
XR_936510.1:n.1786T>A
|
|
|
|
XR_936511.1:n.1786T>A
|
|
|
|
XR_936512.1:n.1661T>A
|
|
|
|
XM_011528653.2:c.1795T>A
|
XP_011526955.1:p.Cys599Ser
|
|
|
XM_011528654.2:c.1669T>A
|
XP_011526956.1:p.Cys557Ser
|
|
|
XR_936510.2:n.1797T>A
|
|
|
|
XR_936511.2:n.1797T>A
|
|
|
|
XR_936512.2:n.1673T>A
|
|
|
|
NM_001207055.2:c.1633T>A
|
NP_001193984.1:p.Cys545Ser
|
|
|
NM_001207056.2:c.1531T>A
|
NP_001193985.1:p.Cys511Ser
|
|
|
NM_006892.4:c.1819T>A
MANE Select
|
NP_008823.1:p.Cys607Ser
|
|
|
NM_175848.2:c.1759T>A
|
NP_787044.1:p.Cys587Ser
|
|
|
NM_175849.2:c.1759T>A
|
NP_787045.1:p.Cys587Ser
|
|
|
NM_175850.3:c.1795T>A
|
NP_787046.1:p.Cys599Ser
|
|
