ENST00000573725.2:c.6769T>G
|
ENSP00000460849.2:p.Phe2257Val
|
|
ENST00000703537.1:c.2697T>G
|
|
|
ENST00000703538.1:c.*6672T>G
|
ENSP00000515361.1:n.*6672T>G
|
|
ENST00000703539.1:n.3263T>G
|
|
|
ENST00000703540.1:c.6802T>G
|
ENSP00000515362.1:p.Phe2268Val
|
|
ENST00000703541.1:c.6814T>G
|
ENSP00000515363.1:p.Phe2272Val
|
|
ENST00000304992.11:c.6949T>G
MANE Select
|
ENSP00000304350.6:p.Phe2317Val
|
|
ENST00000304992.10:c.6949T>G
|
ENSP00000304350.6:p.Phe2317Val
|
|
ENST00000571958.1:c.163-15T>G
|
|
|
ENST00000572621.5:c.6949T>G
|
ENSP00000460348.1:p.Phe2317Val
|
|
ENST00000572723.1:n.938T>G
|
|
|
NM_006445.3:c.6949T>G
|
NP_006436.3:p.Phe2317Val
|
|
XM_024450537.1:c.6949T>G
|
XP_024306305.1:p.Phe2317Val
|
|
NM_006445.4:c.6949T>G
MANE Select
|
NP_006436.3:p.Phe2317Val
|
|