ENST00000262367.10:c.5997C=
MANE Select
|
ENSP00000262367.5:p.Ser1999=
|
|
ENST00000262367.9:c.5997C=
|
ENSP00000262367.5:p.Ser1999=
|
|
ENST00000382070.7:c.5883C=
|
ENSP00000371502.3:p.Ser1961=
|
|
NM_001079846.1:c.5883C=
|
NP_001073315.1:p.Ser1961=
|
|
NM_004380.2:c.5997C=
|
NP_004371.2:p.Ser1999=
|
|
XM_005255124.3:c.5952C=
|
XP_005255181.1:p.Ser1984=
|
|
XM_005255125.3:c.5580C=
|
XP_005255182.1:p.Ser1860=
|
|
XM_006720848.2:c.5736C=
|
XP_006720911.1:p.Ser1912=
|
|
XM_011522380.1:c.5943C=
|
XP_011520682.1:p.Ser1981=
|
|
XM_011522381.1:c.5244C=
|
XP_011520683.1:p.Ser1748=
|
|
XM_005255124.4:c.5952C=
|
XP_005255181.1:p.Ser1984=
|
|
XM_005255125.4:c.5580C=
|
XP_005255182.1:p.Ser1860=
|
|
XM_006720848.3:c.5736C=
|
XP_006720911.1:p.Ser1912=
|
|
XM_011522381.2:c.5244C=
|
XP_011520683.1:p.Ser1748=
|
|
XM_017022944.1:c.5991C=
|
XP_016878433.1:p.Ser1997=
|
|
NM_004380.3:c.5997C=
MANE Select
|
NP_004371.2:p.Ser1999=
|
|