ENST00000592092.2:n.233A>G
|
|
|
ENST00000673918.2:c.5861A>G
|
ENSP00000501283.1:p.Asp1954Gly
|
|
ENST00000674114.2:c.3468A>G
|
ENSP00000501039.2:n.3468A>G
|
|
ENST00000684977.1:c.1145A>G
|
ENSP00000509384.1:p.Asp382Gly
|
|
ENST00000689544.1:n.1080A>G
|
|
|
ENST00000691421.1:c.1148A>G
|
ENSP00000508674.1:p.Asp383Gly
|
|
ENST00000691855.1:c.5469A>G
|
|
|
ENST00000692961.1:c.5927A>G
|
ENSP00000509289.1:p.Asp1976Gly
|
|
ENST00000693677.1:c.704+147A>G
|
ENSP00000509779.1:n.704+147A>G
|
|
ENST00000420124.4:c.5927A>G
MANE Select
|
ENSP00000398837.2:p.Asp1976Gly
|
|
ENST00000673918.1:c.5861A>G
|
ENSP00000501283.1:p.Asp1954Gly
|
|
ENST00000674114.1:c.3249A>G
|
|
|
ENST00000420124.2:c.5927A>G
|
ENSP00000398837.1:p.Asp1976Gly
|
|
NM_014727.2:c.5927A>G
|
NP_055542.1:p.Asp1976Gly
|
|
XM_011527561.1:c.5861A>G
|
XP_011525863.1:p.Asp1954Gly
|
|
XM_011527562.1:c.5927A>G
|
XP_011525864.1:p.Asp1976Gly
|
|
XM_011527563.1:c.5651A>G
|
XP_011525865.1:p.Asp1884Gly
|
|
XM_011527561.2:c.5363A>G
|
XP_011525863.2:p.Asp1788Gly
|
|
XM_011527562.2:c.5927A>G
|
XP_011525864.1:p.Asp1976Gly
|
|
XM_017027544.1:c.5927A>G
|
XP_016883033.1:p.Asp1976Gly
|
|
XM_017027545.1:c.5363A>G
|
XP_016883034.1:p.Asp1788Gly
|
|
XM_017027546.1:c.2891A>G
|
XP_016883035.1:p.Asp964Gly
|
|
NM_014727.3:c.5927A>G
MANE Select
|
NP_055542.1:p.Asp1976Gly
|
|