ENST00000682565.1:c.11556C>A
|
ENSP00000507671.1:p.Asn3852Lys
|
|
ENST00000682801.1:c.11167-926C>A
|
ENSP00000507862.1:n.11167-926C>A
|
|
ENST00000682859.1:c.11556C>A
|
ENSP00000508222.1:p.Asn3852Lys
|
|
ENST00000683791.1:c.4642C>A
|
|
|
ENST00000684460.1:c.8837C>A
|
|
|
ENST00000684548.1:c.11556C>A
|
ENSP00000507421.1:p.Asn3852Lys
|
|
ENST00000684590.1:c.6003C>A
|
ENSP00000507376.1:p.Asn2001Lys
|
|
ENST00000684656.1:c.9021C>A
|
|
|
ENST00000613296.6:c.11937C>A
MANE Select
|
ENSP00000482968.1:p.Asn3979Lys
|
|
ENST00000651057.1:c.2091C>A
|
ENSP00000498504.1:p.Asn697Lys
|
|
ENST00000651434.1:c.3293C>A
|
|
|
ENST00000651750.1:c.1260+378C>A
|
|
|
ENST00000652487.1:c.3108C>A
|
|
|
ENST00000464408.3:n.112C>A
|
|
|
ENST00000484298.5:c.11811C>A
|
ENSP00000478155.1:p.Asn3937Lys
|
|
ENST00000613296.4:c.11937C>A
|
ENSP00000482968.1:p.Asn3979Lys
|
|
ENST00000620466.4:n.5740C>A
|
|
|
NM_015120.4:c.11940C>A , LRG_741t1:c.11940C>A
|
NP_055935.4:p.Asn3980Lys
|
|
NM_001378454.1:c.11937C>A
MANE Select
|
NP_001365383.1:p.Asn3979Lys
|
|