ENST00000592092.2:n.552C>G
|
|
|
ENST00000673918.2:c.6180C>G
|
ENSP00000501283.1:p.Gly2060=
|
|
ENST00000674114.2:c.3787C>G
|
ENSP00000501039.2:n.3787C>G
|
|
ENST00000684977.1:c.1464C>G
|
ENSP00000509384.1:p.Gly488=
|
|
ENST00000689544.1:n.1399C>G
|
|
|
ENST00000691421.1:c.1467C>G
|
ENSP00000508674.1:p.Gly489=
|
|
ENST00000691855.1:c.5788C>G
|
|
|
ENST00000692961.1:c.6246C>G
|
ENSP00000509289.1:p.Gly2082=
|
|
ENST00000693677.1:c.704+466C>G
|
ENSP00000509779.1:n.704+466C>G
|
|
ENST00000420124.4:c.6246C>G
MANE Select
|
ENSP00000398837.2:p.Gly2082=
|
|
ENST00000673918.1:c.6180C>G
|
ENSP00000501283.1:p.Gly2060=
|
|
ENST00000674114.1:c.3568C>G
|
|
|
ENST00000420124.2:c.6246C>G
|
ENSP00000398837.1:p.Gly2082=
|
|
NM_014727.2:c.6246C>G
|
NP_055542.1:p.Gly2082=
|
|
XM_011527561.1:c.6180C>G
|
XP_011525863.1:p.Gly2060=
|
|
XM_011527562.1:c.6246C>G
|
XP_011525864.1:p.Gly2082=
|
|
XM_011527563.1:c.5970C>G
|
XP_011525865.1:p.Gly1990=
|
|
XM_011527561.2:c.5682C>G
|
XP_011525863.2:p.Gly1894=
|
|
XM_011527562.2:c.6246C>G
|
XP_011525864.1:p.Gly2082=
|
|
XM_017027544.1:c.6246C>G
|
XP_016883033.1:p.Gly2082=
|
|
XM_017027545.1:c.5682C>G
|
XP_016883034.1:p.Gly1894=
|
|
XM_017027546.1:c.3210C>G
|
XP_016883035.1:p.Gly1070=
|
|
NM_014727.3:c.6246C>G
MANE Select
|
NP_055542.1:p.Gly2082=
|
|