ENST00000578493.2:n.751G>A
|
|
|
ENST00000699291.1:c.543G>A
|
ENSP00000514272.1:p.Glu181=
|
|
ENST00000699292.1:n.458G>A
|
|
|
ENST00000225275.4:c.1418G>A
MANE Select
|
ENSP00000225275.3:p.Arg473Lys
|
|
ENST00000225275.3:c.1418G>A
|
ENSP00000225275.3:p.Arg473Lys
|
|
NM_000250.1:c.1418G>A , LRG_84t1:c.1418G>A
|
NP_000241.1:p.Arg473Lys
|
|
XM_011524821.1:c.1604G>A
|
XP_011523123.1:p.Arg535Lys
|
|
XM_011524822.1:c.1133G>A
|
XP_011523124.1:p.Arg378Lys
|
|
XM_011524823.1:c.1443G>A
|
XP_011523125.1:p.Glu481=
|
|
NM_000250.2:c.1418G>A
MANE Select
|
NP_000241.1:p.Arg473Lys
|
|