ENST00000480188.2:n.1527A>C
|
|
|
ENST00000696279.1:c.4813A>C
|
|
|
ENST00000696280.1:n.4582A>C
|
|
|
ENST00000696281.1:c.4511A>C
|
ENSP00000512521.1:p.Tyr1504Ser
|
|
ENST00000697921.1:n.3371A>C
|
|
|
ENST00000697922.1:c.*4483A>C
|
ENSP00000513478.1:n.*4483A>C
|
|
ENST00000697923.1:n.4938A>C
|
|
|
ENST00000223642.3:c.4493A>C
MANE Select
|
ENSP00000223642.1:p.Tyr1498Ser
|
|
ENST00000223642.2:c.4493A>C
|
ENSP00000223642.1:p.Tyr1498Ser
|
|
ENST00000480188.1:n.26A>C
|
|
|
NM_001735.2:c.4493A>C , LRG_28t1:c.4493A>C
|
NP_001726.2:p.Tyr1498Ser
|
|
XM_011518980.1:c.4508A>C
|
XP_011517282.1:p.Tyr1503Ser
|
|
NM_001317163.1:c.4511A>C
|
NP_001304092.1:p.Tyr1504Ser
|
|
NM_001317163.2:c.4511A>C
|
NP_001304092.1:p.Tyr1504Ser
|
|
NM_001735.3:c.4493A>C
MANE Select
|
NP_001726.2:p.Tyr1498Ser
|
|