ENST00000695651.1:n.2687T>A
|
|
|
ENST00000695653.1:c.2248T>A
|
ENSP00000512084.1:p.Tyr750Asn
|
|
ENST00000695654.1:c.3364T>A
|
ENSP00000512085.1:p.Tyr1122Asn
|
|
ENST00000695689.1:c.310T>A
|
ENSP00000512101.1:n.310T>A
|
|
ENST00000695690.1:n.530T>A
|
|
|
ENST00000695691.1:n.530T>A
|
|
|
ENST00000245907.11:c.4339T>A
MANE Select
|
ENSP00000245907.4:p.Tyr1447Asn
|
|
ENST00000245907.10:c.4339T>A
|
ENSP00000245907.4:p.Tyr1447Asn
|
|
ENST00000596548.1:c.460T>A
|
ENSP00000469744.1:p.Tyr154Asn
|
|
ENST00000599899.5:n.1298T>A
|
|
|
ENST00000601008.1:c.242-3994T>A
|
ENSP00000471384.1:n.242-3994T>A
|
|
NM_000064.3:c.4339T>A
|
NP_000055.2:p.Tyr1447Asn
|
|
NM_000064.4:c.4339T>A
MANE Select
|
NP_000055.2:p.Tyr1447Asn
|
|