ENST00000218099.7:c.548T>A
MANE Select
|
ENSP00000218099.2:p.Val183Asp
|
|
ENST00000643157.1:n.1215T>A
|
|
|
ENST00000218099.6:c.548T>A
|
ENSP00000218099.2:p.Val183Asp
|
|
ENST00000394090.2:c.434T>A
|
ENSP00000377650.2:p.Val145Asp
|
|
NM_000133.3:c.548T>A , LRG_556t1:c.548T>A
|
NP_000124.1:p.Val183Asp
|
|
NM_001313913.1:c.434T>A
|
NP_001300842.1:p.Val145Asp
|
|
XM_005262397.3:c.419T>A
|
XP_005262454.1:p.Val140Asp
|
|
XM_005262397.4:c.419T>A
|
XP_005262454.1:p.Val140Asp
|
|
NM_000133.4:c.548T>A
MANE Select
|
NP_000124.1:p.Val183Asp
|
|
NM_001313913.2:c.434T>A
|
NP_001300842.1:p.Val145Asp
|
|