ENST00000262367.10:c.7146C>G
MANE Select
|
ENSP00000262367.5:p.Ser2382=
|
|
ENST00000262367.9:c.7146C>G
|
ENSP00000262367.5:p.Ser2382=
|
|
ENST00000382070.7:c.7032C>G
|
ENSP00000371502.3:p.Ser2344=
|
|
NM_001079846.1:c.7032C>G
|
NP_001073315.1:p.Ser2344=
|
|
NM_004380.2:c.7146C>G
|
NP_004371.2:p.Ser2382=
|
|
XM_005255124.3:c.7101C>G
|
XP_005255181.1:p.Ser2367=
|
|
XM_005255125.3:c.6729C>G
|
XP_005255182.1:p.Ser2243=
|
|
XM_006720848.2:c.6885C>G
|
XP_006720911.1:p.Ser2295=
|
|
XM_011522380.1:c.7092C>G
|
XP_011520682.1:p.Ser2364=
|
|
XM_011522381.1:c.6393C>G
|
XP_011520683.1:p.Ser2131=
|
|
XM_005255124.4:c.7101C>G
|
XP_005255181.1:p.Ser2367=
|
|
XM_005255125.4:c.6729C>G
|
XP_005255182.1:p.Ser2243=
|
|
XM_006720848.3:c.6885C>G
|
XP_006720911.1:p.Ser2295=
|
|
XM_011522381.2:c.6393C>G
|
XP_011520683.1:p.Ser2131=
|
|
XM_017022944.1:c.7140C>G
|
XP_016878433.1:p.Ser2380=
|
|
NM_004380.3:c.7146C>G
MANE Select
|
NP_004371.2:p.Ser2382=
|
|