ENST00000378823.8:c.2878G>T
MANE Select
|
ENSP00000368100.4:p.Asp960Tyr
|
|
ENST00000638452.2:c.2581G>T
|
ENSP00000492349.2:p.Asp861Tyr
|
|
ENST00000638504.1:n.2486G>T
|
|
|
ENST00000638568.2:c.2581G>T
|
ENSP00000491158.2:p.Asp861Tyr
|
|
ENST00000639899.1:n.3397G>T
|
|
|
ENST00000640655.2:c.2581G>T
|
ENSP00000491596.2:p.Asp861Tyr
|
|
ENST00000651160.1:c.*1022G>T
|
ENSP00000498829.1:n.*1022G>T
|
|
ENST00000651723.1:c.*2961G>T
|
ENSP00000498237.1:n.*2961G>T
|
|
ENST00000378823.7:c.2878G>T
|
ENSP00000368100.4:p.Asp960Tyr
|
|
ENST00000423956.5:c.*1064G>T
|
ENSP00000390971.1:n.*1064G>T
|
|
ENST00000533482.5:c.*2504G>T
|
ENSP00000431225.1:n.*2504G>T
|
|
NM_005732.3:c.2878G>T
|
NP_005723.2:p.Asp960Tyr
|
|
NM_005732.4:c.2878G>T
MANE Select
|
NP_005723.2:p.Asp960Tyr
|
|