ENST00000695651.1:n.2672A>G
|
|
|
ENST00000695653.1:c.2233A>G
|
ENSP00000512084.1:p.Asn745Asp
|
|
ENST00000695654.1:c.3349A>G
|
ENSP00000512085.1:p.Asn1117Asp
|
|
ENST00000695689.1:c.295A>G
|
ENSP00000512101.1:n.295A>G
|
|
ENST00000695690.1:n.515A>G
|
|
|
ENST00000695691.1:n.515A>G
|
|
|
ENST00000245907.11:c.4324A>G
MANE Select
|
ENSP00000245907.4:p.Asn1442Asp
|
|
ENST00000245907.10:c.4324A>G
|
ENSP00000245907.4:p.Asn1442Asp
|
|
ENST00000596548.1:c.445A>G
|
ENSP00000469744.1:p.Asn149Asp
|
|
ENST00000599899.5:n.1283A>G
|
|
|
ENST00000601008.1:c.242-4009A>G
|
ENSP00000471384.1:n.242-4009A>G
|
|
NM_000064.3:c.4324A>G
|
NP_000055.2:p.Asn1442Asp
|
|
NM_000064.4:c.4324A>G
MANE Select
|
NP_000055.2:p.Asn1442Asp
|
|