|
NM_001201543.2:c.1044T>A
MANE Select
|
NP_001188472.1:p.Tyr348Ter
|
|
ENST00000404929.6:c.1044T>A
MANE Select
|
ENSP00000385158.1:p.Tyr348Ter
|
|
NM_001201543.1:c.1044T>A
|
NP_001188472.1:p.Tyr348Ter
|
|
NM_032180.2:c.1044T>A
|
NP_115556.2:p.Tyr348Ter
|
|
NM_032180.3:c.1044T>A
|
NP_115556.2:p.Tyr348Ter
|
|
NR_037710.1:n.1090T>A
|
|
|
NR_037710.2:n.1007T>A
|
|
|
ENST00000307507.3:c.*1054T>A
|
ENSP00000303170.3:n.*1054T>A
|
|
ENST00000404929.5:c.1044T>A
|
ENSP00000385158.1:p.Tyr348Ter
|
|
ENST00000405894.3:c.1044T>A
|
ENSP00000385893.3:p.Tyr348Ter
|
|
ENST00000418113.5:c.1031T>A
|
|
|
ENST00000456262.5:c.*559T>A
|
ENSP00000396105.1:n.*559T>A
|
|
XM_017005072.1:c.717T>A
|
XP_016860561.1:p.Tyr239Ter
|
|
XM_017005073.1:c.474T>A
|
XP_016860562.1:p.Tyr158Ter
|
|
XM_017005074.1:c.474T>A
|
XP_016860563.1:p.Tyr158Ter
|
|
XR_001738972.2:n.1045T>A
|
|
|
XR_001738973.2:n.1045T>A
|
|
|
XR_001738974.2:n.1045T>A
|
|
|
XR_001738975.2:n.1045T>A
|
|
|
XR_001738976.1:n.1073T>A
|
|
|
XR_001738977.1:n.1073T>A
|
|
|
XR_939724.1:n.2405T>A
|
|