ENST00000573725.2:c.6601A>G
|
ENSP00000460849.2:p.Met2201Val
|
|
ENST00000703537.1:c.2529A>G
|
|
|
ENST00000703538.1:c.*6504A>G
|
ENSP00000515361.1:n.*6504A>G
|
|
ENST00000703539.1:n.3095A>G
|
|
|
ENST00000703540.1:c.6634A>G
|
ENSP00000515362.1:p.Met2212Val
|
|
ENST00000703541.1:c.6646A>G
|
ENSP00000515363.1:p.Met2216Val
|
|
ENST00000304992.11:c.6781A>G
MANE Select
|
ENSP00000304350.6:p.Met2261Val
|
|
ENST00000304992.10:c.6781A>G
|
ENSP00000304350.6:p.Met2261Val
|
|
ENST00000571958.1:c.90A>G
|
|
|
ENST00000572621.5:c.6781A>G
|
ENSP00000460348.1:p.Met2261Val
|
|
ENST00000572723.1:n.770A>G
|
|
|
NM_006445.3:c.6781A>G
|
NP_006436.3:p.Met2261Val
|
|
XM_024450537.1:c.6781A>G
|
XP_024306305.1:p.Met2261Val
|
|
NM_006445.4:c.6781A>G
MANE Select
|
NP_006436.3:p.Met2261Val
|
|