ENST00000262367.10:c.4425T>G
MANE Select
|
ENSP00000262367.5:p.Pro1475=
|
|
ENST00000262367.9:c.4425T>G
|
ENSP00000262367.5:p.Pro1475=
|
|
ENST00000382070.7:c.4311T>G
|
ENSP00000371502.3:p.Pro1437=
|
|
ENST00000570939.2:c.3060T>G
|
ENSP00000461002.2:p.Pro1020=
|
|
ENST00000571763.5:n.215T>G
|
|
|
ENST00000574740.1:n.246T>G
|
|
|
ENST00000576720.1:n.3248T>G
|
|
|
NM_001079846.1:c.4311T>G
|
NP_001073315.1:p.Pro1437=
|
|
NM_004380.2:c.4425T>G
|
NP_004371.2:p.Pro1475=
|
|
XM_005255124.3:c.4380T>G
|
XP_005255181.1:p.Pro1460=
|
|
XM_005255125.3:c.4008T>G
|
XP_005255182.1:p.Pro1336=
|
|
XM_006720848.2:c.4164T>G
|
XP_006720911.1:p.Pro1388=
|
|
XM_011522380.1:c.4371T>G
|
XP_011520682.1:p.Pro1457=
|
|
XM_011522381.1:c.3672T>G
|
XP_011520683.1:p.Pro1224=
|
|
XM_005255124.4:c.4380T>G
|
XP_005255181.1:p.Pro1460=
|
|
XM_005255125.4:c.4008T>G
|
XP_005255182.1:p.Pro1336=
|
|
XM_006720848.3:c.4164T>G
|
XP_006720911.1:p.Pro1388=
|
|
XM_011522381.2:c.3672T>G
|
XP_011520683.1:p.Pro1224=
|
|
XM_017022944.1:c.4419T>G
|
XP_016878433.1:p.Pro1473=
|
|
NM_004380.3:c.4425T>G
MANE Select
|
NP_004371.2:p.Pro1475=
|
|