ENST00000326003.7:c.489G>A
MANE Select
|
ENSP00000314151.1:p.Glu163=
|
|
ENST00000326003.6:c.489G>A
|
ENSP00000314151.1:p.Glu163=
|
|
ENST00000360617.7:c.489G>A
|
ENSP00000353829.2:p.Glu163=
|
|
ENST00000422986.6:c.*145G>A
|
ENSP00000393628.2:n.*145G>A
|
|
ENST00000593997.5:c.489G>A
|
ENSP00000472907.1:p.Glu163=
|
|
ENST00000595392.5:c.365G>A
|
ENSP00000468912.1:p.Arg122Lys
|
|
ENST00000595952.5:c.360G>A
|
ENSP00000471155.1:p.Glu120=
|
|
ENST00000596185.5:c.*597G>A
|
ENSP00000471648.1:n.*597G>A
|
|
ENST00000596333.1:n.524G>A
|
|
|
ENST00000597286.5:c.378G>A
|
ENSP00000470523.1:p.Glu126=
|
|
ENST00000597483.5:c.360G>A
|
ENSP00000472411.1:p.Glu120=
|
|
ENST00000598145.1:c.473G>A
|
|
|
ENST00000601349.5:n.1768G>A
|
|
|
ENST00000601503.5:c.432G>A
|
ENSP00000472213.1:p.Glu144=
|
|
ENST00000601812.1:n.921G>A
|
|
|
ENST00000617027.4:c.366G>A
|
ENSP00000483513.1:p.Glu122=
|
|
NM_001030047.1:c.489G>A
|
NP_001025218.1:p.Glu163=
|
|
NM_001030048.1:c.360G>A
|
NP_001025219.1:p.Glu120=
|
|
NM_001648.2:c.489G>A
MANE Select
|
NP_001639.1:p.Glu163=
|
|
XM_011526923.1:c.489G>A
|
XP_011525225.1:p.Glu163=
|
|
XM_011526924.1:c.489G>A
|
XP_011525226.1:p.Glu163=
|
|
XR_935817.1:n.524G>A
|
|
|