ENST00000695651.1:n.2615A>G
|
|
|
ENST00000695653.1:c.2176A>G
|
ENSP00000512084.1:p.Asn726Asp
|
|
ENST00000695654.1:c.3292A>G
|
ENSP00000512085.1:p.Asn1098Asp
|
|
ENST00000695689.1:c.238A>G
|
ENSP00000512101.1:n.238A>G
|
|
ENST00000695690.1:n.458A>G
|
|
|
ENST00000695691.1:n.458A>G
|
|
|
ENST00000245907.11:c.4267A>G
MANE Select
|
ENSP00000245907.4:p.Asn1423Asp
|
|
ENST00000245907.10:c.4267A>G
|
ENSP00000245907.4:p.Asn1423Asp
|
|
ENST00000596548.1:c.388A>G
|
ENSP00000469744.1:p.Asn130Asp
|
|
ENST00000599899.5:n.1226A>G
|
|
|
ENST00000601008.1:c.242-4066A>G
|
ENSP00000471384.1:n.242-4066A>G
|
|
NM_000064.3:c.4267A>G
|
NP_000055.2:p.Asn1423Asp
|
|
NM_000064.4:c.4267A>G
MANE Select
|
NP_000055.2:p.Asn1423Asp
|
|