ENST00000456935.7:c.1518G>T
MANE Select
|
ENSP00000395473.2:p.Thr506=
|
|
ENST00000221363.8:c.1515G>T
|
ENSP00000221363.4:p.Thr505=
|
|
ENST00000433513.5:n.124G>T
|
|
|
ENST00000456935.6:c.1518G>T
|
ENSP00000395473.2:p.Thr506=
|
|
ENST00000466794.5:n.1417G>T
|
|
|
ENST00000495617.1:n.694G>T
|
|
|
ENST00000593686.1:c.128G>T
|
|
|
ENST00000595880.5:n.115G>T
|
|
|
NM_000528.3:c.1518G>T
|
NP_000519.2:p.Thr506=
|
|
NM_001173498.1:c.1515G>T
|
NP_001166969.1:p.Thr505=
|
|
XM_005259913.1:c.1521G>T
|
XP_005259970.1:p.Thr507=
|
|
XM_011528017.1:c.417G>T
|
XP_011526319.1:p.Thr139=
|
|
XM_005259913.2:c.1521G>T
|
XP_005259970.1:p.Thr507=
|
|
XM_024451518.1:c.417G>T
|
XP_024307286.1:p.Thr139=
|
|
NM_000528.4:c.1518G>T
MANE Select
|
NP_000519.2:p.Thr506=
|
|
NM_001173498.2:c.1515G>T
|
NP_001166969.1:p.Thr505=
|
|