ENST00000592092.2:n.267T>C
|
|
|
ENST00000673918.2:c.5895T>C
|
ENSP00000501283.1:p.Ser1965=
|
|
ENST00000674114.2:c.3502T>C
|
ENSP00000501039.2:n.3502T>C
|
|
ENST00000684977.1:c.1179T>C
|
ENSP00000509384.1:p.Ser393=
|
|
ENST00000689544.1:n.1114T>C
|
|
|
ENST00000691421.1:c.1182T>C
|
ENSP00000508674.1:p.Ser394=
|
|
ENST00000691855.1:c.5503T>C
|
|
|
ENST00000692961.1:c.5961T>C
|
ENSP00000509289.1:p.Ser1987=
|
|
ENST00000693677.1:c.704+181T>C
|
ENSP00000509779.1:n.704+181T>C
|
|
ENST00000420124.4:c.5961T>C
MANE Select
|
ENSP00000398837.2:p.Ser1987=
|
|
ENST00000673918.1:c.5895T>C
|
ENSP00000501283.1:p.Ser1965=
|
|
ENST00000674114.1:c.3283T>C
|
|
|
ENST00000420124.2:c.5961T>C
|
ENSP00000398837.1:p.Ser1987=
|
|
NM_014727.2:c.5961T>C
|
NP_055542.1:p.Ser1987=
|
|
XM_011527561.1:c.5895T>C
|
XP_011525863.1:p.Ser1965=
|
|
XM_011527562.1:c.5961T>C
|
XP_011525864.1:p.Ser1987=
|
|
XM_011527563.1:c.5685T>C
|
XP_011525865.1:p.Ser1895=
|
|
XM_011527561.2:c.5397T>C
|
XP_011525863.2:p.Ser1799=
|
|
XM_011527562.2:c.5961T>C
|
XP_011525864.1:p.Ser1987=
|
|
XM_017027544.1:c.5961T>C
|
XP_016883033.1:p.Ser1987=
|
|
XM_017027545.1:c.5397T>C
|
XP_016883034.1:p.Ser1799=
|
|
XM_017027546.1:c.2925T>C
|
XP_016883035.1:p.Ser975=
|
|
NM_014727.3:c.5961T>C
MANE Select
|
NP_055542.1:p.Ser1987=
|
|