ENST00000302068.9:c.1096A>T
MANE Select
|
ENSP00000306099.4:p.Asn366Tyr
|
|
ENST00000302068.8:c.1096A>T
|
ENSP00000306099.4:p.Asn366Tyr
|
|
ENST00000502545.5:n.939+344A>T
|
|
|
ENST00000509493.1:c.439A>T
|
ENSP00000426757.1:p.Asn147Tyr
|
|
NM_001184741.1:c.919A>T
|
NP_001171670.1:p.Asn307Tyr
|
|
NM_005141.4:c.1096A>T , LRG_558t1:c.1096A>T
|
NP_005132.2:p.Asn366Tyr
|
|
NM_001382759.1:c.964A>T
|
NP_001369688.1:p.Asn322Tyr
|
|
NM_001382760.1:c.1096A>T
|
NP_001369689.1:p.Asn366Tyr
|
|
NM_001382761.1:c.1096A>T
|
NP_001369690.1:p.Asn366Tyr
|
|
NM_001382762.1:c.796A>T
|
NP_001369691.1:p.Asn266Tyr
|
|
NM_001382763.1:c.1087A>T
|
NP_001369692.1:p.Asn363Tyr
|
|
NM_001382764.1:c.1080+16A>T
|
NP_001369693.1:n.1080+16A>T
|
|
NM_001382765.1:c.1096A>T
|
NP_001369694.1:p.Asn366Tyr
|
|
NM_005141.5:c.1096A>T
MANE Select
|
NP_005132.2:p.Asn366Tyr
|
|