ENST00000394329.9:c.14839G>T
MANE Select
|
ENSP00000377862.4:p.Asp4947Tyr
|
|
ENST00000674496.2:c.9610G>T
|
ENSP00000501473.2:p.Asp3204Tyr
|
|
ENST00000335110.5:c.9556G>T
|
ENSP00000335169.5:p.Asp3186Tyr
|
|
ENST00000394329.7:c.14833G>T
|
ENSP00000377862.3:p.Asp4945Tyr
|
|
NM_001291285.1:c.14836G>T
|
NP_001278214.1:p.Asp4946Tyr
|
|
NM_001291303.1:c.14839G>T
|
NP_001278232.1:p.Asp4947Tyr
|
|
NM_024582.4:c.14833G>T
|
NP_078858.4:p.Asp4945Tyr
|
|
XM_011532236.1:c.14839G>T
|
XP_011530538.1:p.Asp4947Tyr
|
|
XM_011532237.1:c.9610G>T
|
XP_011530539.1:p.Asp3204Tyr
|
|
XM_011532236.2:c.14839G>T
|
XP_011530538.1:p.Asp4947Tyr
|
|
XM_011532237.2:c.9610G>T
|
XP_011530539.1:p.Asp3204Tyr
|
|
NM_001291285.2:c.14836G>T
|
NP_001278214.1:p.Asp4946Tyr
|
|
NM_001291303.3:c.14839G>T
MANE Select
|
NP_001278232.1:p.Asp4947Tyr
|
|
NM_024582.5:c.14833G>T
|
NP_078858.4:p.Asp4945Tyr
|
|
NM_001291285.3:c.14836G>T
|
NP_001278214.1:p.Asp4946Tyr
|
|
NM_024582.6:c.14833G>T
|
NP_078858.4:p.Asp4945Tyr
|
|