ENST00000333213.11:c.979G=
MANE Select
|
ENSP00000327487.6:p.Val327=
|
|
ENST00000434205.8:c.676G=
|
ENSP00000406559.4:p.Val226=
|
|
ENST00000545228.3:c.979G=
|
ENSP00000438169.3:p.Val327=
|
|
ENST00000579449.2:n.778G=
|
|
|
ENST00000580013.6:n.1182G=
|
|
|
ENST00000679370.1:n.1560G=
|
|
|
ENST00000679429.1:c.*437G=
|
ENSP00000505403.1:n.*437G=
|
|
ENST00000679443.1:n.1048G=
|
|
|
ENST00000679782.1:c.979G=
|
ENSP00000505995.1:p.Val327=
|
|
ENST00000679919.1:n.1048G=
|
|
|
ENST00000679928.1:c.*590G=
|
ENSP00000506071.1:n.*590G=
|
|
ENST00000680528.1:n.1004G=
|
|
|
ENST00000680999.1:c.979G=
|
ENSP00000504984.1:p.Val327=
|
|
ENST00000681282.1:c.*225G=
|
ENSP00000506339.1:n.*225G=
|
|
ENST00000333213.10:c.979G=
|
ENSP00000327487.6:p.Val327=
|
|
ENST00000545228.2:c.68G=
|
|
|
ENST00000578415.1:c.939G=
|
|
|
ENST00000583173.5:c.512G=
|
ENSP00000463619.1:p.Arg171=
|
|
NM_207346.2:c.979G=
|
NP_997229.2:p.Val327=
|
|
XM_005257229.2:c.979G=
|
XP_005257286.1:p.Val327=
|
|
XM_006721821.2:c.676G=
|
XP_006721884.1:p.Val226=
|
|
XM_011524616.1:c.979G=
|
XP_011522918.1:p.Val327=
|
|
XM_011524617.1:c.979G=
|
XP_011522919.1:p.Val327=
|
|
XM_011524618.1:c.979G=
|
XP_011522920.1:p.Val327=
|
|
XR_243646.2:n.1009G=
|
|
|
XM_005257229.4:c.979G=
|
XP_005257286.1:p.Val327=
|
|
XR_243646.4:n.1015G=
|
|
|
NM_207346.3:c.979G=
MANE Select
|
NP_997229.2:p.Val327=
|
|