ENST00000255078.8:c.2308G>T
MANE Select
|
ENSP00000255078.4:p.Asp770Tyr
|
|
ENST00000674675.1:c.552G>T
|
|
|
ENST00000674878.1:c.547+5G>T
|
|
|
ENST00000674955.1:c.*1025G>T
|
ENSP00000502463.1:n.*1025G>T
|
|
ENST00000675118.1:c.1796G>T
|
|
|
ENST00000675389.1:n.583G>T
|
|
|
ENST00000675615.1:c.2308G>T
|
ENSP00000502413.1:p.Asp770Tyr
|
|
ENST00000675648.1:n.1683G>T
|
|
|
ENST00000675916.1:c.552G>T
|
|
|
ENST00000676173.1:n.3053G>T
|
|
|
ENST00000676182.1:c.739G>T
|
|
|
ENST00000676228.1:c.*1631G>T
|
ENSP00000502375.1:n.*1631G>T
|
|
ENST00000255078.7:c.2308G>T
|
ENSP00000255078.3:p.Asp770Tyr
|
|
ENST00000539064.5:n.2067G>T
|
|
|
ENST00000543739.5:n.1301G>T
|
|
|
NM_002180.2:c.2308G>T , LRG_250t1:c.2308G>T
|
NP_002171.2:p.Asp770Tyr
|
|
XM_005273974.2:c.1297G>T
|
XP_005274031.1:p.Asp433Tyr
|
|
XM_005273975.2:c.1180G>T
|
XP_005274032.1:p.Asp394Tyr
|
|
XM_011544994.1:c.1075G>T
|
XP_011543296.1:p.Asp359Tyr
|
|
XR_949903.1:n.2410G>T
|
|
|
XM_005273975.3:c.1180G>T
|
XP_005274032.1:p.Asp394Tyr
|
|
XM_017017669.2:c.1297G>T
|
XP_016873158.1:p.Asp433Tyr
|
|
XM_017017670.2:c.1297G>T
|
XP_016873159.1:p.Asp433Tyr
|
|
XR_949903.3:n.2406G>T
|
|
|
NM_002180.3:c.2308G>T
MANE Select
|
NP_002171.2:p.Asp770Tyr
|
|