ENST00000673918.2:c.4866C>A
|
ENSP00000501283.1:p.Cys1622Ter
|
|
ENST00000674114.2:c.2473C>A
|
ENSP00000501039.2:n.2473C>A
|
|
ENST00000684977.1:c.150C>A
|
ENSP00000509384.1:p.Cys50Ter
|
|
ENST00000685168.1:c.358C>A
|
|
|
ENST00000689544.1:n.85C>A
|
|
|
ENST00000691421.1:c.153C>A
|
ENSP00000508674.1:p.Cys51Ter
|
|
ENST00000691855.1:c.4474C>A
|
|
|
ENST00000692961.1:c.4932C>A
|
ENSP00000509289.1:p.Cys1644Ter
|
|
ENST00000420124.4:c.4932C>A
MANE Select
|
ENSP00000398837.2:p.Cys1644Ter
|
|
ENST00000673918.1:c.4866C>A
|
ENSP00000501283.1:p.Cys1622Ter
|
|
ENST00000674114.1:c.2254C>A
|
|
|
ENST00000420124.2:c.4932C>A
|
ENSP00000398837.1:p.Cys1644Ter
|
|
NM_014727.2:c.4932C>A
|
NP_055542.1:p.Cys1644Ter
|
|
XM_011527561.1:c.4866C>A
|
XP_011525863.1:p.Cys1622Ter
|
|
XM_011527562.1:c.4932C>A
|
XP_011525864.1:p.Cys1644Ter
|
|
XM_011527563.1:c.4656C>A
|
XP_011525865.1:p.Cys1552Ter
|
|
XM_011527561.2:c.4368C>A
|
XP_011525863.2:p.Cys1456Ter
|
|
XM_011527562.2:c.4932C>A
|
XP_011525864.1:p.Cys1644Ter
|
|
XM_017027544.1:c.4932C>A
|
XP_016883033.1:p.Cys1644Ter
|
|
XM_017027545.1:c.4368C>A
|
XP_016883034.1:p.Cys1456Ter
|
|
XM_017027546.1:c.1896C>A
|
XP_016883035.1:p.Cys632Ter
|
|
NM_014727.3:c.4932C>A
MANE Select
|
NP_055542.1:p.Cys1644Ter
|
|