|
NM_000660.7:c.897C=
MANE Select
|
NP_000651.3:p.Tyr299=
|
|
ENST00000221930.6:c.897C=
MANE Select
|
ENSP00000221930.4:p.Tyr299=
|
|
NM_000660.5:c.897C=
|
NP_000651.3:p.Tyr299=
|
|
NM_000660.6:c.897C=
|
NP_000651.3:p.Tyr299=
|
|
ENST00000221930.5:c.897C=
|
ENSP00000221930.4:p.Tyr299=
|
|
ENST00000598758.5:c.185C=
|
|
|
ENST00000600196.1:n.209C=
|
|
|
ENST00000600196.2:c.749C=
|
ENSP00000504008.1:p.Thr250=
|
|
ENST00000677934.1:c.671C=
|
ENSP00000504769.1:p.Thr224=
|
|
XM_011527242.1:c.900C=
|
XP_011525544.1:p.Tyr300=
|
|
XM_011527242.2:c.900C=
|
XP_011525544.1:p.Tyr300=
|