ENST00000682587.1:c.309T>G
|
ENSP00000507403.1:p.Pro103=
|
|
ENST00000418600.7:c.567T>G
|
ENSP00000403636.3:p.Pro189=
|
|
ENST00000449372.7:c.567T>G
|
ENSP00000416519.4:p.Pro189=
|
|
ENST00000629380.3:c.567T>G
|
ENSP00000486463.1:p.Pro189=
|
|
ENST00000638142.2:c.567T>G
|
ENSP00000490803.1:p.Pro189=
|
|
ENST00000644458.1:c.567T>G
|
ENSP00000495541.1:p.Pro189=
|
|
ENST00000645250.1:c.390T>G
|
ENSP00000494861.1:p.Pro130=
|
|
ENST00000646630.1:c.567T>G
MANE Select
|
ENSP00000496007.1:p.Pro189=
|
|
ENST00000293748.9:c.522T>G
|
ENSP00000293748.6:p.Pro174=
|
|
ENST00000418600.6:c.567T>G
|
ENSP00000403636.3:p.Pro189=
|
|
ENST00000428982.4:c.390T>G
|
ENSP00000412475.2:p.Pro130=
|
|
ENST00000449372.6:c.567T>G
|
ENSP00000416519.3:p.Pro189=
|
|
ENST00000479510.2:n.762T>G
|
|
|
ENST00000628646.2:c.567T>G
|
ENSP00000486431.1:p.Pro189=
|
|
ENST00000629380.2:c.567T>G
|
ENSP00000486463.1:p.Pro189=
|
|
NM_006772.2:c.567T>G
|
NP_006763.2:p.Pro189=
|
|
NM_001130066.1:c.567T>G
|
NP_001123538.1:p.Pro189=
|
|
NM_001130066.2:c.567T>G
|
NP_001123538.1:p.Pro189=
|
|
NM_006772.3:c.567T>G
MANE Select
|
NP_006763.2:p.Pro189=
|
|