|
NM_207346.3:c.1386A=
MANE Select
|
NP_997229.2:p.Arg462=
|
|
ENST00000333213.11:c.1386A=
MANE Select
|
ENSP00000327487.6:p.Arg462=
|
|
NM_207346.2:c.1386A=
|
NP_997229.2:p.Arg462=
|
|
ENST00000333213.10:c.1386A=
|
ENSP00000327487.6:p.Arg462=
|
|
ENST00000434205.8:c.1083A=
|
ENSP00000406559.4:p.Arg361=
|
|
ENST00000545228.2:c.663A=
|
|
|
ENST00000545228.3:c.1574A=
|
ENSP00000438169.3:p.Glu525=
|
|
ENST00000577197.1:n.134A=
|
|
|
ENST00000577197.2:n.584A=
|
|
|
ENST00000579449.1:n.583A=
|
|
|
ENST00000579449.2:n.2126A=
|
|
|
ENST00000580013.6:n.2530A=
|
|
|
ENST00000679370.1:n.2908A=
|
|
|
ENST00000679429.1:c.*844A=
|
ENSP00000505403.1:n.*844A=
|
|
ENST00000679443.1:n.1455A=
|
|
|
ENST00000679782.1:c.*85A=
|
ENSP00000505995.1:n.*85A=
|
|
ENST00000679919.1:n.1657A=
|
|
|
ENST00000679928.1:c.*1938A=
|
ENSP00000506071.1:n.*1938A=
|
|
ENST00000680528.1:n.2352A=
|
|
|
ENST00000680999.1:c.1599A=
|
ENSP00000504984.1:p.Arg533=
|
|
ENST00000681282.1:c.*1573A=
|
ENSP00000506339.1:n.*1573A=
|
|
XM_005257229.2:c.1574A=
|
XP_005257286.1:p.Glu525=
|
|
XM_005257229.4:c.1574A=
|
XP_005257286.1:p.Glu525=
|
|
XM_006721821.2:c.1271A=
|
XP_006721884.1:p.Glu424=
|
|
XM_011524616.1:c.1501+400A=
|
XP_011522918.1:n.1501+400A=
|
|
XM_011524617.1:c.*12+400A=
|
XP_011522919.1:n.*12+400A=
|
|
XM_011524618.1:c.1313+400A=
|
XP_011522920.1:n.1313+400A=
|
|
XR_001753015.1:n.88-367T=
|
|
|
XR_001753016.1:n.89-331T=
|
|
|
XR_243646.2:n.1618A=
|
|
|
XR_243646.4:n.1624A=
|
|
