ENST00000221930.6:c.918C>A
MANE Select
|
ENSP00000221930.4:p.Leu306=
|
|
ENST00000600196.2:c.770C>A
|
ENSP00000504008.1:p.Ser257Ter
|
|
ENST00000677934.1:c.692C>A
|
ENSP00000504769.1:p.Ser231Ter
|
|
ENST00000221930.5:c.918C>A
|
ENSP00000221930.4:p.Leu306=
|
|
ENST00000598758.5:c.206C>A
|
|
|
ENST00000600196.1:n.230C>A
|
|
|
NM_000660.5:c.918C>A
|
NP_000651.3:p.Leu306=
|
|
XM_011527242.1:c.921C>A
|
XP_011525544.1:p.Leu307=
|
|
NM_000660.6:c.918C>A
|
NP_000651.3:p.Leu306=
|
|
XM_011527242.2:c.921C>A
|
XP_011525544.1:p.Leu307=
|
|
NM_000660.7:c.918C>A
MANE Select
|
NP_000651.3:p.Leu306=
|
|