ENST00000673918.2:c.4963G>T
|
ENSP00000501283.1:p.Asp1655Tyr
|
|
ENST00000674114.2:c.2570G>T
|
ENSP00000501039.2:n.2570G>T
|
|
ENST00000684977.1:c.247G>T
|
ENSP00000509384.1:p.Asp83Tyr
|
|
ENST00000685168.1:c.455G>T
|
|
|
ENST00000689544.1:n.182G>T
|
|
|
ENST00000691421.1:c.250G>T
|
ENSP00000508674.1:p.Asp84Tyr
|
|
ENST00000691855.1:c.4571G>T
|
|
|
ENST00000692961.1:c.5029G>T
|
ENSP00000509289.1:p.Asp1677Tyr
|
|
ENST00000420124.4:c.5029G>T
MANE Select
|
ENSP00000398837.2:p.Asp1677Tyr
|
|
ENST00000673918.1:c.4963G>T
|
ENSP00000501283.1:p.Asp1655Tyr
|
|
ENST00000674114.1:c.2351G>T
|
|
|
ENST00000420124.2:c.5029G>T
|
ENSP00000398837.1:p.Asp1677Tyr
|
|
NM_014727.2:c.5029G>T
|
NP_055542.1:p.Asp1677Tyr
|
|
XM_011527561.1:c.4963G>T
|
XP_011525863.1:p.Asp1655Tyr
|
|
XM_011527562.1:c.5029G>T
|
XP_011525864.1:p.Asp1677Tyr
|
|
XM_011527563.1:c.4753G>T
|
XP_011525865.1:p.Asp1585Tyr
|
|
XM_011527561.2:c.4465G>T
|
XP_011525863.2:p.Asp1489Tyr
|
|
XM_011527562.2:c.5029G>T
|
XP_011525864.1:p.Asp1677Tyr
|
|
XM_017027544.1:c.5029G>T
|
XP_016883033.1:p.Asp1677Tyr
|
|
XM_017027545.1:c.4465G>T
|
XP_016883034.1:p.Asp1489Tyr
|
|
XM_017027546.1:c.1993G>T
|
XP_016883035.1:p.Asp665Tyr
|
|
NM_014727.3:c.5029G>T
MANE Select
|
NP_055542.1:p.Asp1677Tyr
|
|