ENST00000573725.2:c.6800C>A
|
ENSP00000460849.2:p.Ser2267Tyr
|
|
ENST00000703537.1:c.2728C>A
|
|
|
ENST00000703538.1:c.*6703C>A
|
ENSP00000515361.1:n.*6703C>A
|
|
ENST00000703539.1:n.3294C>A
|
|
|
ENST00000703540.1:c.6833C>A
|
ENSP00000515362.1:p.Ser2278Tyr
|
|
ENST00000703541.1:c.6845C>A
|
ENSP00000515363.1:p.Ser2282Tyr
|
|
ENST00000304992.11:c.6980C>A
MANE Select
|
ENSP00000304350.6:p.Ser2327Tyr
|
|
ENST00000304992.10:c.6980C>A
|
ENSP00000304350.6:p.Ser2327Tyr
|
|
ENST00000571958.1:c.179C>A
|
|
|
ENST00000572621.5:c.6980C>A
|
ENSP00000460348.1:p.Ser2327Tyr
|
|
NM_006445.3:c.6980C>A
|
NP_006436.3:p.Ser2327Tyr
|
|
XM_024450537.1:c.6980C>A
|
XP_024306305.1:p.Ser2327Tyr
|
|
NM_006445.4:c.6980C>A
MANE Select
|
NP_006436.3:p.Ser2327Tyr
|
|