ENST00000422447.8:c.876T>A
MANE Select
|
ENSP00000395337.3:p.Pro292=
|
|
ENST00000227157.8:c.*26T>A
|
ENSP00000227157.4:n.*26T>A
|
|
ENST00000375710.7:n.1743T>A
|
|
|
ENST00000379412.9:c.876T>A
|
ENSP00000368722.5:p.Pro292=
|
|
ENST00000396222.6:c.688-81T>A
|
ENSP00000379524.2:n.688-81T>A
|
|
ENST00000422447.7:c.876T>A
|
ENSP00000395337.3:p.Pro292=
|
|
ENST00000430553.6:c.702T>A
|
ENSP00000406172.2:p.Pro234=
|
|
ENST00000538451.1:n.763T>A
|
|
|
ENST00000540430.5:c.963T>A
|
ENSP00000445175.1:p.Pro321=
|
|
ENST00000541097.5:c.*214T>A
|
ENSP00000443362.1:n.*214T>A
|
|
ENST00000542179.1:c.876T>A
|
ENSP00000445331.1:p.Pro292=
|
|
ENST00000545215.5:c.*620T>A
|
ENSP00000442637.1:n.*620T>A
|
|
NM_001135239.1:c.702T>A
|
NP_001128711.1:p.Pro234=
|
|
NM_001165414.1:c.963T>A
|
NP_001158886.1:p.Pro321=
|
|
NM_001165415.1:c.688-81T>A
|
NP_001158887.1:n.688-81T>A
|
|
NM_001165416.1:c.*26T>A
|
NP_001158888.1:n.*26T>A
|
|
NM_005566.3:c.876T>A
|
NP_005557.1:p.Pro292=
|
|
NR_028500.1:n.1030T>A
|
|
|
NM_005566.4:c.876T>A
MANE Select
|
NP_005557.1:p.Pro292=
|
|
NM_001165415.2:c.688-81T>A
|
NP_001158887.1:n.688-81T>A
|
|
NM_001135239.2:c.702T>A
|
NP_001128711.1:p.Pro234=
|
|
NM_001165414.2:c.963T>A
|
NP_001158886.1:p.Pro321=
|
|
NM_001165416.2:c.*26T>A
|
NP_001158888.1:n.*26T>A
|
|
NR_028500.2:n.856T>A
|
|
|