ENST00000592092.2:n.689G>T
|
|
|
ENST00000673918.2:c.6317G>T
|
ENSP00000501283.1:p.Gly2106Val
|
|
ENST00000674114.2:c.3924G>T
|
ENSP00000501039.2:n.3924G>T
|
|
ENST00000684977.1:c.1601G>T
|
ENSP00000509384.1:p.Gly534Val
|
|
ENST00000689544.1:n.1536G>T
|
|
|
ENST00000691421.1:c.1604G>T
|
ENSP00000508674.1:p.Gly535Val
|
|
ENST00000691855.1:c.5925G>T
|
|
|
ENST00000692961.1:c.6383G>T
|
ENSP00000509289.1:p.Gly2128Val
|
|
ENST00000693677.1:c.704+603G>T
|
ENSP00000509779.1:n.704+603G>T
|
|
ENST00000420124.4:c.6383G>T
MANE Select
|
ENSP00000398837.2:p.Gly2128Val
|
|
ENST00000673918.1:c.6317G>T
|
ENSP00000501283.1:p.Gly2106Val
|
|
ENST00000674114.1:c.3705G>T
|
|
|
ENST00000420124.2:c.6383G>T
|
ENSP00000398837.1:p.Gly2128Val
|
|
NM_014727.2:c.6383G>T
|
NP_055542.1:p.Gly2128Val
|
|
XM_011527561.1:c.6317G>T
|
XP_011525863.1:p.Gly2106Val
|
|
XM_011527562.1:c.6383G>T
|
XP_011525864.1:p.Gly2128Val
|
|
XM_011527563.1:c.6107G>T
|
XP_011525865.1:p.Gly2036Val
|
|
XM_011527561.2:c.5819G>T
|
XP_011525863.2:p.Gly1940Val
|
|
XM_011527562.2:c.6383G>T
|
XP_011525864.1:p.Gly2128Val
|
|
XM_017027544.1:c.6383G>T
|
XP_016883033.1:p.Gly2128Val
|
|
XM_017027545.1:c.5819G>T
|
XP_016883034.1:p.Gly1940Val
|
|
XM_017027546.1:c.3347G>T
|
XP_016883035.1:p.Gly1116Val
|
|
NM_014727.3:c.6383G>T
MANE Select
|
NP_055542.1:p.Gly2128Val
|
|