ENST00000360538.7:c.137T>A
MANE Select
|
ENSP00000353735.2:p.Phe46Tyr
|
|
ENST00000680198.1:c.137T>A
|
ENSP00000505143.1:p.Phe46Tyr
|
|
ENST00000681750.1:c.-106T>A
|
ENSP00000506413.1:n.-106T>A
|
|
ENST00000360538.6:c.137T>A
|
ENSP00000353735.2:p.Phe46Tyr
|
|
ENST00000379858.1:c.3+1599T>A
|
ENSP00000369187.1:n.3+1599T>A
|
|
NM_001195622.1:c.3+1599T>A
|
NP_001182551.1:n.3+1599T>A
|
|
NM_005802.4:c.137T>A
|
NP_005793.2:p.Phe46Tyr
|
|
NM_005802.5:c.137T>A
MANE Select
|
NP_005793.2:p.Phe46Tyr
|
|
NM_001195622.2:c.3+1599T>A
|
NP_001182551.1:n.3+1599T>A
|
|