ENST00000592092.2:n.528G=
|
|
|
ENST00000673918.2:c.6156G=
|
ENSP00000501283.1:p.Ala2052=
|
|
ENST00000674114.2:c.3763G=
|
ENSP00000501039.2:n.3763G=
|
|
ENST00000684977.1:c.1440G=
|
ENSP00000509384.1:p.Ala480=
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|
ENST00000689544.1:n.1375G=
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|
|
ENST00000691421.1:c.1443G=
|
ENSP00000508674.1:p.Ala481=
|
|
ENST00000691855.1:c.5764G=
|
|
|
ENST00000692961.1:c.6222G=
|
ENSP00000509289.1:p.Ala2074=
|
|
ENST00000693677.1:c.704+442G=
|
ENSP00000509779.1:n.704+442G=
|
|
ENST00000420124.4:c.6222G=
MANE Select
|
ENSP00000398837.2:p.Ala2074=
|
|
ENST00000673918.1:c.6156G=
|
ENSP00000501283.1:p.Ala2052=
|
|
ENST00000674114.1:c.3544G=
|
|
|
ENST00000420124.2:c.6222G=
|
ENSP00000398837.1:p.Ala2074=
|
|
NM_014727.2:c.6222G=
|
NP_055542.1:p.Ala2074=
|
|
XM_011527561.1:c.6156G=
|
XP_011525863.1:p.Ala2052=
|
|
XM_011527562.1:c.6222G=
|
XP_011525864.1:p.Ala2074=
|
|
XM_011527563.1:c.5946G=
|
XP_011525865.1:p.Ala1982=
|
|
XM_011527561.2:c.5658G=
|
XP_011525863.2:p.Ala1886=
|
|
XM_011527562.2:c.6222G=
|
XP_011525864.1:p.Ala2074=
|
|
XM_017027544.1:c.6222G=
|
XP_016883033.1:p.Ala2074=
|
|
XM_017027545.1:c.5658G=
|
XP_016883034.1:p.Ala1886=
|
|
XM_017027546.1:c.3186G=
|
XP_016883035.1:p.Ala1062=
|
|
NM_014727.3:c.6222G=
MANE Select
|
NP_055542.1:p.Ala2074=
|
|