ENST00000456935.7:c.1097C>T
MANE Select
|
ENSP00000395473.2:p.Ala366Val
|
|
ENST00000221363.8:c.1094C>T
|
ENSP00000221363.4:p.Ala365Val
|
|
ENST00000456935.6:c.1097C>T
|
ENSP00000395473.2:p.Ala366Val
|
|
ENST00000465830.1:n.178C>T
|
|
|
ENST00000466794.5:n.1009-96C>T
|
|
|
ENST00000495617.1:n.280+291C>T
|
|
|
NM_000528.3:c.1097C>T
|
NP_000519.2:p.Ala366Val
|
|
NM_001173498.1:c.1094C>T
|
NP_001166969.1:p.Ala365Val
|
|
XM_005259913.1:c.1100C>T
|
XP_005259970.1:p.Ala367Val
|
|
XM_011528017.1:c.9-96C>T
|
XP_011526319.1:n.9-96C>T
|
|
XM_005259913.2:c.1100C>T
|
XP_005259970.1:p.Ala367Val
|
|
XM_024451518.1:c.9-96C>T
|
XP_024307286.1:n.9-96C>T
|
|
NM_000528.4:c.1097C>T
MANE Select
|
NP_000519.2:p.Ala366Val
|
|
NM_001173498.2:c.1094C>T
|
NP_001166969.1:p.Ala365Val
|
|