|
ENST00000209929.10:c.1414C=
MANE Select
|
ENSP00000209929.8:p.Gln472=
|
|
|
ENST00000209929.9:c.1414C=
|
ENSP00000209929.8:p.Gln472=
|
|
|
ENST00000488431.1:n.406C=
|
|
|
|
ENST00000529935.5:c.1199C=
|
ENSP00000487002.1:n.1199C=
|
|
|
NM_001301347.1:c.754C=
|
NP_001288276.1:p.Gln252=
|
|
|
NM_001460.4:c.1414C=
|
NP_001451.2:p.Gln472=
|
|
|
XR_426768.2:n.1531C=
|
|
|
|
XR_921761.1:n.1531C=
|
|
|
|
XR_922278.1:n.507+38630G=
|
|
|
|
NM_001365900.1:c.1219C=
|
NP_001352829.1:p.Gln407=
|
|
|
NR_158622.1:n.1434C=
|
|
|
|
XR_001737072.2:n.1481C=
|
|
|
|
XR_001738291.2:n.1306+38630G=
|
|
|
|
XR_921761.3:n.1481C=
|
|
|
|
XR_922278.3:n.1306+38630G=
|
|
|
|
NM_001460.5:c.1414C=
MANE Select
|
NP_001451.2:p.Gln472=
|
|
|
NR_160266.1:n.1342C=
|
|
|
|
NM_001301347.2:c.754C=
|
NP_001288276.1:p.Gln252=
|
|
