ENST00000463045.3:c.262A>T
|
ENSP00000481376.2:p.Asn88Tyr
|
|
ENST00000491274.6:c.391A>T
|
ENSP00000480482.2:p.Asn131Tyr
|
|
ENST00000375499.8:c.433A>T
MANE Select
|
ENSP00000364649.3:p.Asn145Tyr
|
|
ENST00000375499.7:c.433A>T
|
ENSP00000364649.3:p.Asn145Tyr
|
|
ENST00000463045.2:c.262A>T
|
ENSP00000481376.1:p.Asn88Tyr
|
|
ENST00000475506.1:n.350A>T
|
|
|
ENST00000485515.5:n.367A>T
|
|
|
ENST00000491274.5:c.391A>T
|
ENSP00000480482.1:p.Asn131Tyr
|
|
NM_003000.2:c.433A>T , LRG_316t1:c.433A>T
|
NP_002991.2:p.Asn145Tyr
|
|
NM_003000.3:c.433A>T
MANE Select
|
NP_002991.2:p.Asn145Tyr
|
|