ENST00000578493.2:n.775C>A
|
|
|
ENST00000699291.1:c.567C>A
|
ENSP00000514272.1:p.Phe189Leu
|
|
ENST00000699292.1:n.482C>A
|
|
|
ENST00000225275.4:c.1442C>A
MANE Select
|
ENSP00000225275.3:p.Ser481Tyr
|
|
ENST00000225275.3:c.1442C>A
|
ENSP00000225275.3:p.Ser481Tyr
|
|
NM_000250.1:c.1442C>A , LRG_84t1:c.1442C>A
|
NP_000241.1:p.Ser481Tyr
|
|
XM_011524821.1:c.1628C>A
|
XP_011523123.1:p.Ser543Tyr
|
|
XM_011524822.1:c.1157C>A
|
XP_011523124.1:p.Ser386Tyr
|
|
XM_011524823.1:c.1467C>A
|
XP_011523125.1:p.Phe489Leu
|
|
NM_000250.2:c.1442C>A
MANE Select
|
NP_000241.1:p.Ser481Tyr
|
|