ENST00000302068.9:c.1094C>A
MANE Select
|
ENSP00000306099.4:p.Ala365Asp
|
|
ENST00000302068.8:c.1094C>A
|
ENSP00000306099.4:p.Ala365Asp
|
|
ENST00000502545.5:n.939+342C>A
|
|
|
ENST00000509493.1:c.437C>A
|
ENSP00000426757.1:p.Ala146Asp
|
|
NM_001184741.1:c.917C>A
|
NP_001171670.1:p.Ala306Asp
|
|
NM_005141.4:c.1094C>A , LRG_558t1:c.1094C>A
|
NP_005132.2:p.Ala365Asp
|
|
NM_001382759.1:c.962C>A
|
NP_001369688.1:p.Ala321Asp
|
|
NM_001382760.1:c.1094C>A
|
NP_001369689.1:p.Ala365Asp
|
|
NM_001382761.1:c.1094C>A
|
NP_001369690.1:p.Ala365Asp
|
|
NM_001382762.1:c.794C>A
|
NP_001369691.1:p.Ala265Asp
|
|
NM_001382763.1:c.1085C>A
|
NP_001369692.1:p.Ala362Asp
|
|
NM_001382764.1:c.1080+14C>A
|
NP_001369693.1:n.1080+14C>A
|
|
NM_001382765.1:c.1094C>A
|
NP_001369694.1:p.Ala365Asp
|
|
NM_005141.5:c.1094C>A
MANE Select
|
NP_005132.2:p.Ala365Asp
|
|