ENST00000470094.2:c.*303T=
|
ENSP00000434898.2:n.*303T=
|
|
ENST00000528762.2:c.*1147T=
|
ENSP00000433168.2:n.*1147T=
|
|
ENST00000530893.7:c.9411T=
|
ENSP00000499438.2:p.Asp3137=
|
|
ENST00000665585.2:c.*1342T=
|
ENSP00000499570.2:n.*1342T=
|
|
ENST00000700202.2:c.9729T=
|
ENSP00000514856.2:p.Asp3243=
|
|
ENST00000700202.1:c.2196T=
|
ENSP00000514856.1:p.Asp732=
|
|
ENST00000700203.1:n.1907T=
|
|
|
ENST00000380152.8:c.9780T=
MANE Select
|
ENSP00000369497.3:p.Asp3260=
|
|
ENST00000544455.6:c.9780T=
|
ENSP00000439902.1:p.Asp3260=
|
|
ENST00000614259.2:c.9788T=
|
ENSP00000506251.1:n.9788T=
|
|
ENST00000680887.1:c.9780T=
|
ENSP00000505508.1:p.Asp3260=
|
|
ENST00000380152.7:c.9780T=
|
ENSP00000369497.3:p.Asp3260=
|
|
ENST00000533776.1:n.368T=
|
|
|
ENST00000544455.5:c.9780T=
|
ENSP00000439902.1:p.Asp3260=
|
|
NM_000059.3:c.9780T= , LRG_293t1:c.9780T=
|
NP_000050.2:p.Asp3260=
|
|
XM_011535203.1:c.9780T=
|
XP_011533505.1:p.Asp3260=
|
|
XM_011535204.1:c.9684T=
|
XP_011533506.1:p.Asp3228=
|
|
NM_000059.4:c.9780T=
MANE Select
|
NP_000050.3:p.Asp3260=
|
|