ENST00000358387.9:c.592G>T
MANE Select
|
ENSP00000351157.5:p.Asp198Tyr
|
|
ENST00000358387.8:c.592G>T
|
ENSP00000351157.4:p.Asp198Tyr
|
|
ENST00000505174.1:n.1315G>T
|
|
|
ENST00000506350.1:n.31G>T
|
|
|
ENST00000507024.5:c.*410G>T
|
ENSP00000424716.1:n.*410G>T
|
|
ENST00000508779.1:c.543G>T
|
|
|
ENST00000511070.5:c.104G>T
|
ENSP00000423609.1:p.Gly35Val
|
|
NM_024715.3:c.592G>T
|
NP_078991.3:p.Asp198Tyr
|
|
NM_001350735.1:c.388G>T
|
NP_001337664.1:p.Asp130Tyr
|
|
NM_024715.4:c.592G>T
MANE Select
|
NP_078991.3:p.Asp198Tyr
|
|
NM_001350735.2:c.388G>T
|
NP_001337664.1:p.Asp130Tyr
|
|