ENST00000695651.1:n.2975T>A
|
|
|
ENST00000695653.1:c.2536T>A
|
ENSP00000512084.1:p.Tyr846Asn
|
|
ENST00000695654.1:c.3652T>A
|
ENSP00000512085.1:p.Tyr1218Asn
|
|
ENST00000695689.1:c.598T>A
|
ENSP00000512101.1:n.598T>A
|
|
ENST00000695690.1:n.1692T>A
|
|
|
ENST00000695691.1:n.1488T>A
|
|
|
ENST00000245907.11:c.4627T>A
MANE Select
|
ENSP00000245907.4:p.Tyr1543Asn
|
|
ENST00000245907.10:c.4627T>A
|
ENSP00000245907.4:p.Tyr1543Asn
|
|
ENST00000599668.1:n.247T>A
|
|
|
ENST00000599899.5:n.1586T>A
|
|
|
ENST00000601008.1:c.242-1170T>A
|
ENSP00000471384.1:n.242-1170T>A
|
|
ENST00000602229.1:c.74T>A
|
|
|
NM_000064.3:c.4627T>A
|
NP_000055.2:p.Tyr1543Asn
|
|
NM_000064.4:c.4627T>A
MANE Select
|
NP_000055.2:p.Tyr1543Asn
|
|