ENST00000221930.6:c.857T>A
MANE Select
|
ENSP00000221930.4:p.Phe286Tyr
|
|
ENST00000600196.2:c.712+284T>A
|
ENSP00000504008.1:n.712+284T>A
|
|
ENST00000677934.1:c.634+2861T>A
|
ENSP00000504769.1:n.634+2861T>A
|
|
ENST00000221930.5:c.857T>A
|
ENSP00000221930.4:p.Phe286Tyr
|
|
ENST00000598758.5:c.145T>A
|
|
|
ENST00000600196.1:n.172+284T>A
|
|
|
NM_000660.5:c.857T>A
|
NP_000651.3:p.Phe286Tyr
|
|
XM_011527242.1:c.860T>A
|
XP_011525544.1:p.Phe287Tyr
|
|
NM_000660.6:c.857T>A
|
NP_000651.3:p.Phe286Tyr
|
|
XM_011527242.2:c.860T>A
|
XP_011525544.1:p.Phe287Tyr
|
|
NM_000660.7:c.857T>A
MANE Select
|
NP_000651.3:p.Phe286Tyr
|
|