ENST00000695651.1:n.2855A>T
|
|
|
ENST00000695653.1:c.2416A>T
|
ENSP00000512084.1:p.Asn806Tyr
|
|
ENST00000695654.1:c.3532A>T
|
ENSP00000512085.1:p.Asn1178Tyr
|
|
ENST00000695689.1:c.478A>T
|
ENSP00000512101.1:n.478A>T
|
|
ENST00000695690.1:n.1572A>T
|
|
|
ENST00000695691.1:n.1368A>T
|
|
|
ENST00000245907.11:c.4507A>T
MANE Select
|
ENSP00000245907.4:p.Asn1503Tyr
|
|
ENST00000245907.10:c.4507A>T
|
ENSP00000245907.4:p.Asn1503Tyr
|
|
ENST00000599668.1:n.102A>T
|
|
|
ENST00000599899.5:n.1466A>T
|
|
|
ENST00000601008.1:c.242-1488A>T
|
ENSP00000471384.1:n.242-1488A>T
|
|
NM_000064.3:c.4507A>T
|
NP_000055.2:p.Asn1503Tyr
|
|
NM_000064.4:c.4507A>T
MANE Select
|
NP_000055.2:p.Asn1503Tyr
|
|