ENST00000578493.2:n.763C>A
|
|
|
ENST00000699291.1:c.555C>A
|
ENSP00000514272.1:p.Ala185=
|
|
ENST00000699292.1:n.470C>A
|
|
|
ENST00000225275.4:c.1430C>A
MANE Select
|
ENSP00000225275.3:p.Pro477His
|
|
ENST00000225275.3:c.1430C>A
|
ENSP00000225275.3:p.Pro477His
|
|
NM_000250.1:c.1430C>A , LRG_84t1:c.1430C>A
|
NP_000241.1:p.Pro477His
|
|
XM_011524821.1:c.1616C>A
|
XP_011523123.1:p.Pro539His
|
|
XM_011524822.1:c.1145C>A
|
XP_011523124.1:p.Pro382His
|
|
XM_011524823.1:c.1455C>A
|
XP_011523125.1:p.Ala485=
|
|
NM_000250.2:c.1430C>A
MANE Select
|
NP_000241.1:p.Pro477His
|
|