ENST00000480188.2:n.1391T>G
|
|
|
ENST00000696279.1:c.4677T>G
|
|
|
ENST00000696280.1:n.4446T>G
|
|
|
ENST00000696281.1:c.4375T>G
|
ENSP00000512521.1:p.Tyr1459Asp
|
|
ENST00000697921.1:n.3235T>G
|
|
|
ENST00000697922.1:c.*4347T>G
|
ENSP00000513478.1:n.*4347T>G
|
|
ENST00000697923.1:n.4802T>G
|
|
|
ENST00000223642.3:c.4357T>G
MANE Select
|
ENSP00000223642.1:p.Tyr1453Asp
|
|
ENST00000223642.2:c.4357T>G
|
ENSP00000223642.1:p.Tyr1453Asp
|
|
NM_001735.2:c.4357T>G , LRG_28t1:c.4357T>G
|
NP_001726.2:p.Tyr1453Asp
|
|
XM_011518980.1:c.4372T>G
|
XP_011517282.1:p.Tyr1458Asp
|
|
NM_001317163.1:c.4375T>G
|
NP_001304092.1:p.Tyr1459Asp
|
|
NM_001317163.2:c.4375T>G
|
NP_001304092.1:p.Tyr1459Asp
|
|
NM_001735.3:c.4357T>G
MANE Select
|
NP_001726.2:p.Tyr1453Asp
|
|