ENST00000348974.5:c.1604T>A
|
ENSP00000330021.7:p.Phe535Tyr
|
|
ENST00000394236.9:c.1604T>A
MANE Select
|
ENSP00000377783.3:p.Phe535Tyr
|
|
ENST00000407433.6:c.1559T>A
|
ENSP00000385794.2:p.Phe520Tyr
|
|
ENST00000647936.1:c.1604T>A
|
ENSP00000496822.1:p.Phe535Tyr
|
|
ENST00000648381.1:n.1772T>A
|
|
|
ENST00000648853.1:c.1562T>A
|
ENSP00000497262.1:p.Phe521Tyr
|
|
ENST00000649103.1:c.1703T>A
|
ENSP00000497962.1:n.1703T>A
|
|
ENST00000649585.1:c.547T>A
|
ENSP00000498163.1:n.547T>A
|
|
ENST00000650591.1:c.1700T>A
|
ENSP00000497376.1:p.Phe567Tyr
|
|
ENST00000394236.7:c.1604T>A
|
ENSP00000377783.3:p.Phe535Tyr
|
|
ENST00000407433.5:c.1211T>A
|
ENSP00000385794.1:p.Phe404Tyr
|
|
NM_000313.3:c.1604T>A , LRG_572t1:c.1604T>A
|
NP_000304.2:p.Phe535Tyr
|
|
NM_001314077.1:c.1700T>A , LRG_572t2:c.1700T>A
|
NP_001301006.1:p.Phe567Tyr
|
|
NM_000313.4:c.1604T>A
MANE Select
|
NP_000304.2:p.Phe535Tyr
|
|
NM_001314077.2:c.1700T>A
|
NP_001301006.1:p.Phe567Tyr
|
|