ENST00000255078.8:c.1775C>T
MANE Select
|
ENSP00000255078.4:p.Ala592Val
|
|
ENST00000674675.1:c.19C>T
|
|
|
ENST00000674878.1:c.19C>T
|
|
|
ENST00000674955.1:c.*492C>T
|
ENSP00000502463.1:n.*492C>T
|
|
ENST00000675118.1:c.1263C>T
|
|
|
ENST00000675389.1:n.50C>T
|
|
|
ENST00000675615.1:c.1775C>T
|
ENSP00000502413.1:p.Ala592Val
|
|
ENST00000675648.1:n.1150C>T
|
|
|
ENST00000675916.1:c.19C>T
|
|
|
ENST00000676173.1:n.2520C>T
|
|
|
ENST00000676182.1:c.206C>T
|
|
|
ENST00000676228.1:c.*1098C>T
|
ENSP00000502375.1:n.*1098C>T
|
|
ENST00000255078.7:c.1775C>T
|
ENSP00000255078.3:p.Ala592Val
|
|
ENST00000539064.5:n.1534C>T
|
|
|
ENST00000541229.5:n.470C>T
|
|
|
ENST00000543739.5:n.768C>T
|
|
|
ENST00000545475.1:n.371C>T
|
|
|
NM_002180.2:c.1775C>T , LRG_250t1:c.1775C>T
|
NP_002171.2:p.Ala592Val
|
|
XM_005273974.2:c.764C>T
|
XP_005274031.1:p.Ala255Val
|
|
XM_005273975.2:c.647C>T
|
XP_005274032.1:p.Ala216Val
|
|
XM_011544994.1:c.542C>T
|
XP_011543296.1:p.Ala181Val
|
|
XR_949903.1:n.1877C>T
|
|
|
XM_005273975.3:c.647C>T
|
XP_005274032.1:p.Ala216Val
|
|
XM_017017669.2:c.764C>T
|
XP_016873158.1:p.Ala255Val
|
|
XM_017017670.2:c.764C>T
|
XP_016873159.1:p.Ala255Val
|
|
XR_949903.3:n.1873C>T
|
|
|
NM_002180.3:c.1775C>T
MANE Select
|
NP_002171.2:p.Ala592Val
|
|