ENST00000578493.2:n.729G>A
|
|
|
ENST00000699291.1:c.521G>A
|
ENSP00000514272.1:p.Gly174Asp
|
|
ENST00000699292.1:n.436G>A
|
|
|
ENST00000225275.4:c.1396G>A
MANE Select
|
ENSP00000225275.3:p.Val466Met
|
|
ENST00000225275.3:c.1396G>A
|
ENSP00000225275.3:p.Val466Met
|
|
NM_000250.1:c.1396G>A , LRG_84t1:c.1396G>A
|
NP_000241.1:p.Val466Met
|
|
XM_011524821.1:c.1582G>A
|
XP_011523123.1:p.Val528Met
|
|
XM_011524822.1:c.1111G>A
|
XP_011523124.1:p.Val371Met
|
|
XM_011524823.1:c.1421G>A
|
XP_011523125.1:p.Gly474Asp
|
|
NM_000250.2:c.1396G>A
MANE Select
|
NP_000241.1:p.Val466Met
|
|