ENST00000262367.10:c.4280+67A=
MANE Select
|
ENSP00000262367.5:n.4280+67A=
|
|
ENST00000262367.9:c.4280+67A=
|
ENSP00000262367.5:n.4280+67A=
|
|
ENST00000382070.7:c.4166+67A=
|
ENSP00000371502.3:n.4166+67A=
|
|
ENST00000570939.2:c.2915+67A=
|
ENSP00000461002.2:n.2915+67A=
|
|
ENST00000573517.6:c.653A=
|
|
|
ENST00000574740.1:n.215+888A=
|
|
|
ENST00000576720.1:n.3217+67A=
|
|
|
NM_001079846.1:c.4166+67A=
|
NP_001073315.1:n.4166+67A=
|
|
NM_004380.2:c.4280+67A=
|
NP_004371.2:n.4280+67A=
|
|
XM_005255124.3:c.4235+67A=
|
XP_005255181.1:n.4235+67A=
|
|
XM_005255125.3:c.3863+67A=
|
XP_005255182.1:n.3863+67A=
|
|
XM_006720848.2:c.4133+888A=
|
XP_006720911.1:n.4133+888A=
|
|
XM_011522380.1:c.4226+67A=
|
XP_011520682.1:n.4226+67A=
|
|
XM_011522381.1:c.3527+67A=
|
XP_011520683.1:n.3527+67A=
|
|
XM_005255124.4:c.4235+67A=
|
XP_005255181.1:n.4235+67A=
|
|
XM_005255125.4:c.3863+67A=
|
XP_005255182.1:n.3863+67A=
|
|
XM_006720848.3:c.4133+888A=
|
XP_006720911.1:n.4133+888A=
|
|
XM_011522381.2:c.3527+67A=
|
XP_011520683.1:n.3527+67A=
|
|
XM_017022944.1:c.4274+67A=
|
XP_016878433.1:n.4274+67A=
|
|
NM_004380.3:c.4280+67A=
MANE Select
|
NP_004371.2:n.4280+67A=
|
|