ENST00000262367.10:c.4272A>G
MANE Select
|
ENSP00000262367.5:p.Pro1424=
|
|
ENST00000262367.9:c.4272A>G
|
ENSP00000262367.5:p.Pro1424=
|
|
ENST00000382070.7:c.4158A>G
|
ENSP00000371502.3:p.Pro1386=
|
|
ENST00000570939.2:c.2907A>G
|
ENSP00000461002.2:p.Pro969=
|
|
ENST00000573517.6:c.578A>G
|
|
|
ENST00000574740.1:n.215+813A>G
|
|
|
ENST00000576720.1:n.3209A>G
|
|
|
NM_001079846.1:c.4158A>G
|
NP_001073315.1:p.Pro1386=
|
|
NM_004380.2:c.4272A>G
|
NP_004371.2:p.Pro1424=
|
|
XM_005255124.3:c.4227A>G
|
XP_005255181.1:p.Pro1409=
|
|
XM_005255125.3:c.3855A>G
|
XP_005255182.1:p.Pro1285=
|
|
XM_006720848.2:c.4133+813A>G
|
XP_006720911.1:n.4133+813A>G
|
|
XM_011522380.1:c.4218A>G
|
XP_011520682.1:p.Pro1406=
|
|
XM_011522381.1:c.3519A>G
|
XP_011520683.1:p.Pro1173=
|
|
XM_005255124.4:c.4227A>G
|
XP_005255181.1:p.Pro1409=
|
|
XM_005255125.4:c.3855A>G
|
XP_005255182.1:p.Pro1285=
|
|
XM_006720848.3:c.4133+813A>G
|
XP_006720911.1:n.4133+813A>G
|
|
XM_011522381.2:c.3519A>G
|
XP_011520683.1:p.Pro1173=
|
|
XM_017022944.1:c.4266A>G
|
XP_016878433.1:p.Pro1422=
|
|
NM_004380.3:c.4272A>G
MANE Select
|
NP_004371.2:p.Pro1424=
|
|