ENST00000573725.2:c.6472T>G
|
ENSP00000460849.2:p.Phe2158Val
|
|
ENST00000703537.1:c.2400T>G
|
|
|
ENST00000703538.1:c.*6375T>G
|
ENSP00000515361.1:n.*6375T>G
|
|
ENST00000703539.1:n.2966T>G
|
|
|
ENST00000703540.1:c.6505T>G
|
ENSP00000515362.1:p.Phe2169Val
|
|
ENST00000703541.1:c.6517T>G
|
ENSP00000515363.1:p.Phe2173Val
|
|
ENST00000304992.11:c.6652T>G
MANE Select
|
ENSP00000304350.6:p.Phe2218Val
|
|
ENST00000304992.10:c.6652T>G
|
ENSP00000304350.6:p.Phe2218Val
|
|
ENST00000572621.5:c.6652T>G
|
ENSP00000460348.1:p.Phe2218Val
|
|
ENST00000572723.1:n.641T>G
|
|
|
NM_006445.3:c.6652T>G
|
NP_006436.3:p.Phe2218Val
|
|
XM_024450537.1:c.6652T>G
|
XP_024306305.1:p.Phe2218Val
|
|
NM_006445.4:c.6652T>G
MANE Select
|
NP_006436.3:p.Phe2218Val
|
|