ENST00000302068.9:c.1234A>T
MANE Select
|
ENSP00000306099.4:p.Asn412Tyr
|
|
ENST00000302068.8:c.1234A>T
|
ENSP00000306099.4:p.Asn412Tyr
|
|
ENST00000502545.5:n.939+482A>T
|
|
|
ENST00000509493.1:c.577A>T
|
ENSP00000426757.1:p.Asn193Tyr
|
|
NM_001184741.1:c.1057A>T
|
NP_001171670.1:p.Asn353Tyr
|
|
NM_005141.4:c.1234A>T , LRG_558t1:c.1234A>T
|
NP_005132.2:p.Asn412Tyr
|
|
NM_001382759.1:c.1102A>T
|
NP_001369688.1:p.Asn368Tyr
|
|
NM_001382760.1:c.1234A>T
|
NP_001369689.1:p.Asn412Tyr
|
|
NM_001382761.1:c.1234A>T
|
NP_001369690.1:p.Asn412Tyr
|
|
NM_001382762.1:c.934A>T
|
NP_001369691.1:p.Asn312Tyr
|
|
NM_001382763.1:c.1225A>T
|
NP_001369692.1:p.Asn409Tyr
|
|
NM_001382764.1:c.*8A>T
|
NP_001369693.1:n.*8A>T
|
|
NM_001382765.1:c.1220+14A>T
|
NP_001369694.1:n.1220+14A>T
|
|
NM_005141.5:c.1234A>T
MANE Select
|
NP_005132.2:p.Asn412Tyr
|
|