ENST00000262367.10:c.6051T>G
MANE Select
|
ENSP00000262367.5:p.Pro2017=
|
|
ENST00000262367.9:c.6051T>G
|
ENSP00000262367.5:p.Pro2017=
|
|
ENST00000382070.7:c.5937T>G
|
ENSP00000371502.3:p.Pro1979=
|
|
NM_001079846.1:c.5937T>G
|
NP_001073315.1:p.Pro1979=
|
|
NM_004380.2:c.6051T>G
|
NP_004371.2:p.Pro2017=
|
|
XM_005255124.3:c.6006T>G
|
XP_005255181.1:p.Pro2002=
|
|
XM_005255125.3:c.5634T>G
|
XP_005255182.1:p.Pro1878=
|
|
XM_006720848.2:c.5790T>G
|
XP_006720911.1:p.Pro1930=
|
|
XM_011522380.1:c.5997T>G
|
XP_011520682.1:p.Pro1999=
|
|
XM_011522381.1:c.5298T>G
|
XP_011520683.1:p.Pro1766=
|
|
XM_005255124.4:c.6006T>G
|
XP_005255181.1:p.Pro2002=
|
|
XM_005255125.4:c.5634T>G
|
XP_005255182.1:p.Pro1878=
|
|
XM_006720848.3:c.5790T>G
|
XP_006720911.1:p.Pro1930=
|
|
XM_011522381.2:c.5298T>G
|
XP_011520683.1:p.Pro1766=
|
|
XM_017022944.1:c.6045T>G
|
XP_016878433.1:p.Pro2015=
|
|
NM_004380.3:c.6051T>G
MANE Select
|
NP_004371.2:p.Pro2017=
|
|