ENST00000470094.2:c.*569C>A
|
ENSP00000434898.2:n.*569C>A
|
|
ENST00000528762.2:c.*1413C>A
|
ENSP00000433168.2:n.*1413C>A
|
|
ENST00000530893.7:c.9677C>A
|
ENSP00000499438.2:p.Thr3226Asn
|
|
ENST00000665585.2:c.*1608C>A
|
ENSP00000499570.2:n.*1608C>A
|
|
ENST00000700202.2:c.9995C>A
|
ENSP00000514856.2:p.Thr3332Asn
|
|
ENST00000700202.1:c.2462C>A
|
ENSP00000514856.1:p.Thr821Asn
|
|
ENST00000700203.1:n.2173C>A
|
|
|
ENST00000380152.8:c.10046C>A
MANE Select
|
ENSP00000369497.3:p.Thr3349Asn
|
|
ENST00000544455.6:c.10046C>A
|
ENSP00000439902.1:p.Thr3349Asn
|
|
ENST00000614259.2:c.10054C>A
|
ENSP00000506251.1:n.10054C>A
|
|
ENST00000680887.1:c.10046C>A
|
ENSP00000505508.1:p.Thr3349Asn
|
|
ENST00000380152.7:c.10046C>A
|
ENSP00000369497.3:p.Thr3349Asn
|
|
ENST00000544455.5:c.10046C>A
|
ENSP00000439902.1:p.Thr3349Asn
|
|
NM_000059.3:c.10046C>A , LRG_293t1:c.10046C>A
|
NP_000050.2:p.Thr3349Asn
|
|
XM_011535203.1:c.10046C>A
|
XP_011533505.1:p.Thr3349Asn
|
|
XM_011535204.1:c.9950C>A
|
XP_011533506.1:p.Thr3317Asn
|
|
NM_000059.4:c.10046C>A
MANE Select
|
NP_000050.3:p.Thr3349Asn
|
|