ENST00000642498.1:c.1013T>A
|
ENSP00000493631.1:p.Leu338His
|
|
ENST00000642538.1:c.*357T>A
|
ENSP00000493927.1:n.*357T>A
|
|
ENST00000643188.1:c.1013T>A
|
ENSP00000493903.1:p.Leu338His
|
|
ENST00000643443.1:c.*720T>A
|
ENSP00000495572.1:n.*720T>A
|
|
ENST00000643502.1:c.670T>A
|
|
|
ENST00000643908.1:n.1231T>A
|
|
|
ENST00000644538.1:n.1290T>A
|
|
|
ENST00000644793.1:c.1013T>A
|
ENSP00000495750.1:p.Leu338His
|
|
ENST00000645328.1:c.391T>A
|
|
|
ENST00000645408.1:c.546T>A
|
|
|
ENST00000645723.1:n.2252T>A
|
|
|
ENST00000646405.1:c.*431T>A
|
ENSP00000493744.1:n.*431T>A
|
|
ENST00000646512.1:n.1159T>A
|
|
|
ENST00000646735.1:c.680T>A
|
ENSP00000493763.1:p.Leu227His
|
|
ENST00000651619.1:c.1013T>A
MANE Select
|
ENSP00000498303.1:p.Leu338His
|
|
ENST00000216951.6:c.1013T>A
|
ENSP00000216951.2:p.Leu338His
|
|
ENST00000451957.2:c.680T>A
|
ENSP00000407517.2:p.Leu227His
|
|
NM_000178.2:c.1013T>A
|
NP_000169.1:p.Leu338His
|
|
XM_005260406.3:c.1013T>A
|
XP_005260463.1:p.Leu338His
|
|
XM_011528796.1:c.1013T>A
|
XP_011527098.1:p.Leu338His
|
|
NM_000178.4:c.1013T>A
MANE Select
|
NP_000169.1:p.Leu338His
|
|
NM_001322494.1:c.1013T>A
|
NP_001309423.1:p.Leu338His
|
|
NM_001322495.1:c.1013T>A
|
NP_001309424.1:p.Leu338His
|
|