ENST00000592092.2:n.258A>T
|
|
|
ENST00000673918.2:c.5886A>T
|
ENSP00000501283.1:p.Ser1962=
|
|
ENST00000674114.2:c.3493A>T
|
ENSP00000501039.2:n.3493A>T
|
|
ENST00000684977.1:c.1170A>T
|
ENSP00000509384.1:p.Ser390=
|
|
ENST00000689544.1:n.1105A>T
|
|
|
ENST00000691421.1:c.1173A>T
|
ENSP00000508674.1:p.Ser391=
|
|
ENST00000691855.1:c.5494A>T
|
|
|
ENST00000692961.1:c.5952A>T
|
ENSP00000509289.1:p.Ser1984=
|
|
ENST00000693677.1:c.704+172A>T
|
ENSP00000509779.1:n.704+172A>T
|
|
ENST00000420124.4:c.5952A>T
MANE Select
|
ENSP00000398837.2:p.Ser1984=
|
|
ENST00000673918.1:c.5886A>T
|
ENSP00000501283.1:p.Ser1962=
|
|
ENST00000674114.1:c.3274A>T
|
|
|
ENST00000420124.2:c.5952A>T
|
ENSP00000398837.1:p.Ser1984=
|
|
NM_014727.2:c.5952A>T
|
NP_055542.1:p.Ser1984=
|
|
XM_011527561.1:c.5886A>T
|
XP_011525863.1:p.Ser1962=
|
|
XM_011527562.1:c.5952A>T
|
XP_011525864.1:p.Ser1984=
|
|
XM_011527563.1:c.5676A>T
|
XP_011525865.1:p.Ser1892=
|
|
XM_011527561.2:c.5388A>T
|
XP_011525863.2:p.Ser1796=
|
|
XM_011527562.2:c.5952A>T
|
XP_011525864.1:p.Ser1984=
|
|
XM_017027544.1:c.5952A>T
|
XP_016883033.1:p.Ser1984=
|
|
XM_017027545.1:c.5388A>T
|
XP_016883034.1:p.Ser1796=
|
|
XM_017027546.1:c.2916A>T
|
XP_016883035.1:p.Ser972=
|
|
NM_014727.3:c.5952A>T
MANE Select
|
NP_055542.1:p.Ser1984=
|
|