ENST00000367990.7:c.265T>G
MANE Select
|
ENSP00000356969.3:p.Tyr89Asp
|
|
ENST00000463273.5:c.265T>G
|
ENSP00000476740.1:p.Tyr89Asp
|
|
ENST00000463812.1:c.121T>G
|
ENSP00000476890.1:p.Tyr41Asp
|
|
ENST00000464492.5:c.364T>G
|
ENSP00000476911.1:p.Tyr122Asp
|
|
ENST00000468465.5:c.121T>G
|
ENSP00000476662.1:p.Tyr41Asp
|
|
ENST00000470459.6:c.211T>G
|
ENSP00000477031.1:p.Tyr71Asp
|
|
ENST00000481413.1:n.776T>G
|
|
|
ENST00000481511.5:c.*262T>G
|
ENSP00000477054.1:n.*262T>G
|
|
ENST00000491350.1:c.*48T>G
|
ENSP00000477353.1:n.*48T>G
|
|
NM_001643.1:c.265T>G
|
NP_001634.1:p.Tyr89Asp
|
|
NM_001643.2:c.265T>G
MANE Select
|
NP_001634.1:p.Tyr89Asp
|
|