ENST00000255078.8:c.2069C>T
MANE Select
|
ENSP00000255078.4:p.Ala690Val
|
|
ENST00000674675.1:c.313C>T
|
|
|
ENST00000674878.1:c.313C>T
|
|
|
ENST00000674955.1:c.*786C>T
|
ENSP00000502463.1:n.*786C>T
|
|
ENST00000675118.1:c.1557C>T
|
|
|
ENST00000675389.1:n.344C>T
|
|
|
ENST00000675615.1:c.2069C>T
|
ENSP00000502413.1:p.Ala690Val
|
|
ENST00000675648.1:n.1444C>T
|
|
|
ENST00000675916.1:c.313C>T
|
|
|
ENST00000676173.1:n.2814C>T
|
|
|
ENST00000676182.1:c.500C>T
|
|
|
ENST00000676228.1:c.*1392C>T
|
ENSP00000502375.1:n.*1392C>T
|
|
ENST00000255078.7:c.2069C>T
|
ENSP00000255078.3:p.Ala690Val
|
|
ENST00000539064.5:n.1828C>T
|
|
|
ENST00000543739.5:n.1062C>T
|
|
|
NM_002180.2:c.2069C>T , LRG_250t1:c.2069C>T
|
NP_002171.2:p.Ala690Val
|
|
XM_005273974.2:c.1058C>T
|
XP_005274031.1:p.Ala353Val
|
|
XM_005273975.2:c.941C>T
|
XP_005274032.1:p.Ala314Val
|
|
XM_011544994.1:c.836C>T
|
XP_011543296.1:p.Ala279Val
|
|
XR_949903.1:n.2171C>T
|
|
|
XM_005273975.3:c.941C>T
|
XP_005274032.1:p.Ala314Val
|
|
XM_017017669.2:c.1058C>T
|
XP_016873158.1:p.Ala353Val
|
|
XM_017017670.2:c.1058C>T
|
XP_016873159.1:p.Ala353Val
|
|
XR_949903.3:n.2167C>T
|
|
|
NM_002180.3:c.2069C>T
MANE Select
|
NP_002171.2:p.Ala690Val
|
|