ENST00000592092.2:n.695G>A
|
|
|
ENST00000673918.2:c.6323G>A
|
ENSP00000501283.1:p.Gly2108Asp
|
|
ENST00000674114.2:c.3930G>A
|
ENSP00000501039.2:n.3930G>A
|
|
ENST00000684977.1:c.1607G>A
|
ENSP00000509384.1:p.Gly536Asp
|
|
ENST00000689544.1:n.1542G>A
|
|
|
ENST00000691421.1:c.1610G>A
|
ENSP00000508674.1:p.Gly537Asp
|
|
ENST00000691855.1:c.5931G>A
|
|
|
ENST00000692961.1:c.6389G>A
|
ENSP00000509289.1:p.Gly2130Asp
|
|
ENST00000693677.1:c.704+609G>A
|
ENSP00000509779.1:n.704+609G>A
|
|
ENST00000420124.4:c.6389G>A
MANE Select
|
ENSP00000398837.2:p.Gly2130Asp
|
|
ENST00000673918.1:c.6323G>A
|
ENSP00000501283.1:p.Gly2108Asp
|
|
ENST00000674114.1:c.3711G>A
|
|
|
ENST00000420124.2:c.6389G>A
|
ENSP00000398837.1:p.Gly2130Asp
|
|
NM_014727.2:c.6389G>A
|
NP_055542.1:p.Gly2130Asp
|
|
XM_011527561.1:c.6323G>A
|
XP_011525863.1:p.Gly2108Asp
|
|
XM_011527562.1:c.6389G>A
|
XP_011525864.1:p.Gly2130Asp
|
|
XM_011527563.1:c.6113G>A
|
XP_011525865.1:p.Gly2038Asp
|
|
XM_011527561.2:c.5825G>A
|
XP_011525863.2:p.Gly1942Asp
|
|
XM_011527562.2:c.6389G>A
|
XP_011525864.1:p.Gly2130Asp
|
|
XM_017027544.1:c.6389G>A
|
XP_016883033.1:p.Gly2130Asp
|
|
XM_017027545.1:c.5825G>A
|
XP_016883034.1:p.Gly1942Asp
|
|
XM_017027546.1:c.3353G>A
|
XP_016883035.1:p.Gly1118Asp
|
|
NM_014727.3:c.6389G>A
MANE Select
|
NP_055542.1:p.Gly2130Asp
|
|