ENST00000578493.2:n.859T>A
|
|
|
ENST00000699291.1:c.651T>A
|
ENSP00000514272.1:n.651T>A
|
|
ENST00000699292.1:n.566T>A
|
|
|
ENST00000225275.4:c.1526T>A
MANE Select
|
ENSP00000225275.3:p.Met509Lys
|
|
ENST00000225275.3:c.1526T>A
|
ENSP00000225275.3:p.Met509Lys
|
|
NM_000250.1:c.1526T>A , LRG_84t1:c.1526T>A
|
NP_000241.1:p.Met509Lys
|
|
XM_011524821.1:c.1712T>A
|
XP_011523123.1:p.Met571Lys
|
|
XM_011524822.1:c.1241T>A
|
XP_011523124.1:p.Met414Lys
|
|
XM_011524823.1:c.*75T>A
|
XP_011523125.1:n.*75T>A
|
|
NM_000250.2:c.1526T>A
MANE Select
|
NP_000241.1:p.Met509Lys
|
|