ENST00000288774.8:c.213G>T
|
ENSP00000288774.3:p.Glu71Asp
|
|
ENST00000447513.7:c.213G>T
MANE Select
|
ENSP00000407922.2:p.Glu71Asp
|
|
ENST00000650293.1:c.167G>T
|
|
|
ENST00000288774.7:c.213G>T
|
ENSP00000288774.3:p.Glu71Asp
|
|
ENST00000447513.6:c.213G>T
|
ENSP00000407922.2:p.Glu71Asp
|
|
ENST00000502666.1:c.418G>T
|
ENSP00000461951.1:n.418G>T
|
|
ENST00000507596.5:c.213G>T
|
ENSP00000424291.1:p.Glu71Asp
|
|
ENST00000508384.5:c.-220G>T
|
ENSP00000464289.1:n.-220G>T
|
|
ENST00000510434.1:c.213G>T
|
ENSP00000423051.1:p.Glu71Asp
|
|
ENST00000514502.1:c.*230G>T
|
ENSP00000425924.1:n.*230G>T
|
|
ENST00000515760.1:n.347G>T
|
|
|
NM_002617.3:c.213G>T
|
NP_002608.1:p.Glu71Asp
|
|
NM_153818.1:c.213G>T
|
NP_722540.1:p.Glu71Asp
|
|
XM_011541573.1:c.213G>T
|
XP_011539875.1:p.Glu71Asp
|
|
XM_011541574.1:c.-220G>T
|
XP_011539876.1:n.-220G>T
|
|
XM_011541575.1:c.-220G>T
|
XP_011539877.1:n.-220G>T
|
|
XM_011541576.1:c.213G>T
|
XP_011539878.1:p.Glu71Asp
|
|
XR_946666.1:n.333G>T
|
|
|
XM_011541576.2:c.213G>T
|
XP_011539878.1:p.Glu71Asp
|
|
XR_946666.2:n.282G>T
|
|
|
NM_001374425.1:c.213G>T
|
NP_001361354.1:p.Glu71Asp
|
|
NM_001374426.1:c.-220G>T
|
NP_001361355.1:n.-220G>T
|
|
NM_001374427.1:c.-220G>T
|
NP_001361356.1:n.-220G>T
|
|
NM_002617.4:c.213G>T
MANE Select
|
NP_002608.1:p.Glu71Asp
|
|
NM_153818.2:c.213G>T
|
NP_722540.1:p.Glu71Asp
|
|
NR_164636.1:n.332G>T
|
|
|