ENST00000592092.2:n.598G>T
|
|
|
ENST00000673918.2:c.6226G>T
|
ENSP00000501283.1:p.Ala2076Ser
|
|
ENST00000674114.2:c.3833G>T
|
ENSP00000501039.2:n.3833G>T
|
|
ENST00000684977.1:c.1510G>T
|
ENSP00000509384.1:p.Ala504Ser
|
|
ENST00000689544.1:n.1445G>T
|
|
|
ENST00000691421.1:c.1513G>T
|
ENSP00000508674.1:p.Ala505Ser
|
|
ENST00000691855.1:c.5834G>T
|
|
|
ENST00000692961.1:c.6292G>T
|
ENSP00000509289.1:p.Ala2098Ser
|
|
ENST00000693677.1:c.704+512G>T
|
ENSP00000509779.1:n.704+512G>T
|
|
ENST00000420124.4:c.6292G>T
MANE Select
|
ENSP00000398837.2:p.Ala2098Ser
|
|
ENST00000673918.1:c.6226G>T
|
ENSP00000501283.1:p.Ala2076Ser
|
|
ENST00000674114.1:c.3614G>T
|
|
|
ENST00000420124.2:c.6292G>T
|
ENSP00000398837.1:p.Ala2098Ser
|
|
NM_014727.2:c.6292G>T
|
NP_055542.1:p.Ala2098Ser
|
|
XM_011527561.1:c.6226G>T
|
XP_011525863.1:p.Ala2076Ser
|
|
XM_011527562.1:c.6292G>T
|
XP_011525864.1:p.Ala2098Ser
|
|
XM_011527563.1:c.6016G>T
|
XP_011525865.1:p.Ala2006Ser
|
|
XM_011527561.2:c.5728G>T
|
XP_011525863.2:p.Ala1910Ser
|
|
XM_011527562.2:c.6292G>T
|
XP_011525864.1:p.Ala2098Ser
|
|
XM_017027544.1:c.6292G>T
|
XP_016883033.1:p.Ala2098Ser
|
|
XM_017027545.1:c.5728G>T
|
XP_016883034.1:p.Ala1910Ser
|
|
XM_017027546.1:c.3256G>T
|
XP_016883035.1:p.Ala1086Ser
|
|
NM_014727.3:c.6292G>T
MANE Select
|
NP_055542.1:p.Ala2098Ser
|
|