ENST00000480188.2:n.1397A>G
|
|
|
ENST00000696279.1:c.4683A>G
|
|
|
ENST00000696280.1:n.4452A>G
|
|
|
ENST00000696281.1:c.4381A>G
|
ENSP00000512521.1:p.Ile1461Val
|
|
ENST00000697921.1:n.3241A>G
|
|
|
ENST00000697922.1:c.*4353A>G
|
ENSP00000513478.1:n.*4353A>G
|
|
ENST00000697923.1:n.4808A>G
|
|
|
ENST00000223642.3:c.4363A>G
MANE Select
|
ENSP00000223642.1:p.Ile1455Val
|
|
ENST00000223642.2:c.4363A>G
|
ENSP00000223642.1:p.Ile1455Val
|
|
NM_001735.2:c.4363A>G , LRG_28t1:c.4363A>G
|
NP_001726.2:p.Ile1455Val
|
|
XM_011518980.1:c.4378A>G
|
XP_011517282.1:p.Ile1460Val
|
|
NM_001317163.1:c.4381A>G
|
NP_001304092.1:p.Ile1461Val
|
|
NM_001317163.2:c.4381A>G
|
NP_001304092.1:p.Ile1461Val
|
|
NM_001735.3:c.4363A>G
MANE Select
|
NP_001726.2:p.Ile1455Val
|
|