ENST00000578493.2:n.729G>T
|
|
|
ENST00000699291.1:c.521G>T
|
ENSP00000514272.1:p.Gly174Val
|
|
ENST00000699292.1:n.436G>T
|
|
|
ENST00000225275.4:c.1396G>T
MANE Select
|
ENSP00000225275.3:p.Val466Leu
|
|
ENST00000225275.3:c.1396G>T
|
ENSP00000225275.3:p.Val466Leu
|
|
NM_000250.1:c.1396G>T , LRG_84t1:c.1396G>T
|
NP_000241.1:p.Val466Leu
|
|
XM_011524821.1:c.1582G>T
|
XP_011523123.1:p.Val528Leu
|
|
XM_011524822.1:c.1111G>T
|
XP_011523124.1:p.Val371Leu
|
|
XM_011524823.1:c.1421G>T
|
XP_011523125.1:p.Gly474Val
|
|
NM_000250.2:c.1396G>T
MANE Select
|
NP_000241.1:p.Val466Leu
|
|