ENST00000262367.10:c.7292C>G
MANE Select
|
ENSP00000262367.5:p.Thr2431Arg
|
|
ENST00000262367.9:c.7292C>G
|
ENSP00000262367.5:p.Thr2431Arg
|
|
ENST00000382070.7:c.7178C>G
|
ENSP00000371502.3:p.Thr2393Arg
|
|
NM_001079846.1:c.7178C>G
|
NP_001073315.1:p.Thr2393Arg
|
|
NM_004380.2:c.7292C>G
|
NP_004371.2:p.Thr2431Arg
|
|
XM_005255124.3:c.7247C>G
|
XP_005255181.1:p.Thr2416Arg
|
|
XM_005255125.3:c.6875C>G
|
XP_005255182.1:p.Thr2292Arg
|
|
XM_006720848.2:c.7031C>G
|
XP_006720911.1:p.Thr2344Arg
|
|
XM_011522380.1:c.7238C>G
|
XP_011520682.1:p.Thr2413Arg
|
|
XM_011522381.1:c.6539C>G
|
XP_011520683.1:p.Thr2180Arg
|
|
XM_005255124.4:c.7247C>G
|
XP_005255181.1:p.Thr2416Arg
|
|
XM_005255125.4:c.6875C>G
|
XP_005255182.1:p.Thr2292Arg
|
|
XM_006720848.3:c.7031C>G
|
XP_006720911.1:p.Thr2344Arg
|
|
XM_011522381.2:c.6539C>G
|
XP_011520683.1:p.Thr2180Arg
|
|
XM_017022944.1:c.7286C>G
|
XP_016878433.1:p.Thr2429Arg
|
|
NM_004380.3:c.7292C>G
MANE Select
|
NP_004371.2:p.Thr2431Arg
|
|