ENST00000255078.8:c.2135T>A
MANE Select
|
ENSP00000255078.4:p.Leu712His
|
|
ENST00000674675.1:c.379T>A
|
|
|
ENST00000674878.1:c.379T>A
|
|
|
ENST00000674955.1:c.*852T>A
|
ENSP00000502463.1:n.*852T>A
|
|
ENST00000675118.1:c.1623T>A
|
|
|
ENST00000675389.1:n.410T>A
|
|
|
ENST00000675615.1:c.2135T>A
|
ENSP00000502413.1:p.Leu712His
|
|
ENST00000675648.1:n.1510T>A
|
|
|
ENST00000675916.1:c.379T>A
|
|
|
ENST00000676173.1:n.2880T>A
|
|
|
ENST00000676182.1:c.566T>A
|
|
|
ENST00000676228.1:c.*1458T>A
|
ENSP00000502375.1:n.*1458T>A
|
|
ENST00000255078.7:c.2135T>A
|
ENSP00000255078.3:p.Leu712His
|
|
ENST00000539064.5:n.1894T>A
|
|
|
ENST00000543739.5:n.1128T>A
|
|
|
NM_002180.2:c.2135T>A , LRG_250t1:c.2135T>A
|
NP_002171.2:p.Leu712His
|
|
XM_005273974.2:c.1124T>A
|
XP_005274031.1:p.Leu375His
|
|
XM_005273975.2:c.1007T>A
|
XP_005274032.1:p.Leu336His
|
|
XM_011544994.1:c.902T>A
|
XP_011543296.1:p.Leu301His
|
|
XR_949903.1:n.2237T>A
|
|
|
XM_005273975.3:c.1007T>A
|
XP_005274032.1:p.Leu336His
|
|
XM_017017669.2:c.1124T>A
|
XP_016873158.1:p.Leu375His
|
|
XM_017017670.2:c.1124T>A
|
XP_016873159.1:p.Leu375His
|
|
XR_949903.3:n.2233T>A
|
|
|
NM_002180.3:c.2135T>A
MANE Select
|
NP_002171.2:p.Leu712His
|
|