ENST00000592092.2:n.672G>A
|
|
|
ENST00000673918.2:c.6300G>A
|
ENSP00000501283.1:p.Gly2100=
|
|
ENST00000674114.2:c.3907G>A
|
ENSP00000501039.2:n.3907G>A
|
|
ENST00000684977.1:c.1584G>A
|
ENSP00000509384.1:p.Gly528=
|
|
ENST00000689544.1:n.1519G>A
|
|
|
ENST00000691421.1:c.1587G>A
|
ENSP00000508674.1:p.Gly529=
|
|
ENST00000691855.1:c.5908G>A
|
|
|
ENST00000692961.1:c.6366G>A
|
ENSP00000509289.1:p.Gly2122=
|
|
ENST00000693677.1:c.704+586G>A
|
ENSP00000509779.1:n.704+586G>A
|
|
ENST00000420124.4:c.6366G>A
MANE Select
|
ENSP00000398837.2:p.Gly2122=
|
|
ENST00000673918.1:c.6300G>A
|
ENSP00000501283.1:p.Gly2100=
|
|
ENST00000674114.1:c.3688G>A
|
|
|
ENST00000420124.2:c.6366G>A
|
ENSP00000398837.1:p.Gly2122=
|
|
NM_014727.2:c.6366G>A
|
NP_055542.1:p.Gly2122=
|
|
XM_011527561.1:c.6300G>A
|
XP_011525863.1:p.Gly2100=
|
|
XM_011527562.1:c.6366G>A
|
XP_011525864.1:p.Gly2122=
|
|
XM_011527563.1:c.6090G>A
|
XP_011525865.1:p.Gly2030=
|
|
XM_011527561.2:c.5802G>A
|
XP_011525863.2:p.Gly1934=
|
|
XM_011527562.2:c.6366G>A
|
XP_011525864.1:p.Gly2122=
|
|
XM_017027544.1:c.6366G>A
|
XP_016883033.1:p.Gly2122=
|
|
XM_017027545.1:c.5802G>A
|
XP_016883034.1:p.Gly1934=
|
|
XM_017027546.1:c.3330G>A
|
XP_016883035.1:p.Gly1110=
|
|
NM_014727.3:c.6366G>A
MANE Select
|
NP_055542.1:p.Gly2122=
|
|