ENST00000545399.6:c.932T>A
|
ENSP00000444688.1:p.Ile311Asn
|
|
ENST00000644613.1:c.893T>A
|
ENSP00000494711.1:p.Ile298Asn
|
|
ENST00000648268.1:c.893T>A
MANE Select
|
ENSP00000498113.1:p.Ile298Asn
|
|
ENST00000302102.9:c.893T>A
|
ENSP00000302397.5:p.Ile298Asn
|
|
ENST00000441343.5:c.893T>A
|
ENSP00000411503.1:p.Ile298Asn
|
|
ENST00000485672.2:n.206T>A
|
|
|
ENST00000543770.5:c.926T>A
|
ENSP00000437577.1:p.Ile309Asn
|
|
ENST00000545399.5:c.932T>A
|
ENSP00000444688.1:p.Ile311Asn
|
|
ENST00000602133.5:c.803T>A
|
ENSP00000471581.1:p.Ile268Asn
|
|
NM_001256213.1:c.926T>A
|
NP_001243142.1:p.Ile309Asn
|
|
NM_001256214.1:c.932T>A
|
NP_001243143.1:p.Ile311Asn
|
|
NM_152296.4:c.893T>A
|
NP_689509.1:p.Ile298Asn
|
|
XM_011526991.1:c.803T>A
|
XP_011525293.1:p.Ile268Asn
|
|
NM_152296.5:c.893T>A
MANE Select
|
NP_689509.1:p.Ile298Asn
|
|
NM_001256214.2:c.932T>A
|
NP_001243143.1:p.Ile311Asn
|
|
NM_001256213.2:c.926T>A
|
NP_001243142.1:p.Ile309Asn
|
|