|
ENST00000696231.1:c.*938G>T
|
ENSP00000512497.1:n.*938G>T
|
|
|
ENST00000696232.1:c.1987G>T
|
ENSP00000512498.1:p.Gly663Cys
|
|
|
ENST00000696233.1:c.*730G>T
|
ENSP00000512499.1:n.*730G>T
|
|
|
ENST00000696238.1:c.*730G>T
|
ENSP00000512502.1:n.*730G>T
|
|
|
ENST00000696239.1:c.1768G>T
|
ENSP00000512503.1:p.Gly590Cys
|
|
|
ENST00000696245.1:n.82G>T
|
|
|
|
ENST00000201963.3:c.1963G>T
|
ENSP00000201963.3:p.Gly655Cys
|
|
|
ENST00000328111.6:c.1987G>T
MANE Select
|
ENSP00000328547.2:p.Gly663Cys
|
|
|
ENST00000348286.6:c.1927G>T
|
ENSP00000337764.2:p.Gly643Cys
|
|
|
ENST00000353855.6:c.1927G>T
|
ENSP00000313397.4:p.Gly643Cys
|
|
|
ENST00000443239.7:c.1801G>T
|
ENSP00000403169.2:p.Gly601Cys
|
|
|
ENST00000456297.6:c.1699G>T
|
ENSP00000412305.1:p.Gly567Cys
|
|
|
NM_001207055.1:c.1801G>T
|
NP_001193984.1:p.Gly601Cys
|
|
|
NM_001207056.1:c.1699G>T
|
NP_001193985.1:p.Gly567Cys
|
|
|
NM_006892.3:c.1987G>T , LRG_56t1:c.1987G>T
|
NP_008823.1:p.Gly663Cys
|
|
|
NM_175848.1:c.1927G>T
|
NP_787044.1:p.Gly643Cys
|
|
|
NM_175849.1:c.1927G>T
|
NP_787045.1:p.Gly643Cys
|
|
|
NM_175850.2:c.1963G>T
|
NP_787046.1:p.Gly655Cys
|
|
|
XM_011528653.1:c.1963G>T
|
XP_011526955.1:p.Gly655Cys
|
|
|
XM_011528654.1:c.1837G>T
|
XP_011526956.1:p.Gly613Cys
|
|
|
XR_936510.1:n.1954G>T
|
|
|
|
XR_936511.1:n.1954G>T
|
|
|
|
XR_936512.1:n.1829G>T
|
|
|
|
XM_011528653.2:c.1963G>T
|
XP_011526955.1:p.Gly655Cys
|
|
|
XM_011528654.2:c.1837G>T
|
XP_011526956.1:p.Gly613Cys
|
|
|
XR_936510.2:n.1965G>T
|
|
|
|
XR_936511.2:n.1965G>T
|
|
|
|
XR_936512.2:n.1841G>T
|
|
|
|
NM_001207055.2:c.1801G>T
|
NP_001193984.1:p.Gly601Cys
|
|
|
NM_001207056.2:c.1699G>T
|
NP_001193985.1:p.Gly567Cys
|
|
|
NM_006892.4:c.1987G>T
MANE Select
|
NP_008823.1:p.Gly663Cys
|
|
|
NM_175848.2:c.1927G>T
|
NP_787044.1:p.Gly643Cys
|
|
|
NM_175849.2:c.1927G>T
|
NP_787045.1:p.Gly643Cys
|
|
|
NM_175850.3:c.1963G>T
|
NP_787046.1:p.Gly655Cys
|
|
