ENST00000673918.2:c.4881C>T
|
ENSP00000501283.1:p.Ala1627=
|
|
ENST00000674114.2:c.2488C>T
|
ENSP00000501039.2:n.2488C>T
|
|
ENST00000684977.1:c.165C>T
|
ENSP00000509384.1:p.Ala55=
|
|
ENST00000685168.1:c.373C>T
|
|
|
ENST00000689544.1:n.100C>T
|
|
|
ENST00000691421.1:c.168C>T
|
ENSP00000508674.1:p.Ala56=
|
|
ENST00000691855.1:c.4489C>T
|
|
|
ENST00000692961.1:c.4947C>T
|
ENSP00000509289.1:p.Ala1649=
|
|
ENST00000420124.4:c.4947C>T
MANE Select
|
ENSP00000398837.2:p.Ala1649=
|
|
ENST00000673918.1:c.4881C>T
|
ENSP00000501283.1:p.Ala1627=
|
|
ENST00000674114.1:c.2269C>T
|
|
|
ENST00000420124.2:c.4947C>T
|
ENSP00000398837.1:p.Ala1649=
|
|
NM_014727.2:c.4947C>T
|
NP_055542.1:p.Ala1649=
|
|
XM_011527561.1:c.4881C>T
|
XP_011525863.1:p.Ala1627=
|
|
XM_011527562.1:c.4947C>T
|
XP_011525864.1:p.Ala1649=
|
|
XM_011527563.1:c.4671C>T
|
XP_011525865.1:p.Ala1557=
|
|
XM_011527561.2:c.4383C>T
|
XP_011525863.2:p.Ala1461=
|
|
XM_011527562.2:c.4947C>T
|
XP_011525864.1:p.Ala1649=
|
|
XM_017027544.1:c.4947C>T
|
XP_016883033.1:p.Ala1649=
|
|
XM_017027545.1:c.4383C>T
|
XP_016883034.1:p.Ala1461=
|
|
XM_017027546.1:c.1911C>T
|
XP_016883035.1:p.Ala637=
|
|
NM_014727.3:c.4947C>T
MANE Select
|
NP_055542.1:p.Ala1649=
|
|