ENST00000470094.2:c.*324G=
|
ENSP00000434898.2:n.*324G=
|
|
ENST00000528762.2:c.*1168G=
|
ENSP00000433168.2:n.*1168G=
|
|
ENST00000530893.7:c.9432G=
|
ENSP00000499438.2:p.Lys3144=
|
|
ENST00000665585.2:c.*1363G=
|
ENSP00000499570.2:n.*1363G=
|
|
ENST00000700202.2:c.9750G=
|
ENSP00000514856.2:p.Lys3250=
|
|
ENST00000700202.1:c.2217G=
|
ENSP00000514856.1:p.Lys739=
|
|
ENST00000700203.1:n.1928G=
|
|
|
ENST00000380152.8:c.9801G=
MANE Select
|
ENSP00000369497.3:p.Lys3267=
|
|
ENST00000544455.6:c.9801G=
|
ENSP00000439902.1:p.Lys3267=
|
|
ENST00000614259.2:c.9809G=
|
ENSP00000506251.1:n.9809G=
|
|
ENST00000680887.1:c.9801G=
|
ENSP00000505508.1:p.Lys3267=
|
|
ENST00000380152.7:c.9801G=
|
ENSP00000369497.3:p.Lys3267=
|
|
ENST00000533776.1:n.389G=
|
|
|
ENST00000544455.5:c.9801G=
|
ENSP00000439902.1:p.Lys3267=
|
|
NM_000059.3:c.9801G= , LRG_293t1:c.9801G=
|
NP_000050.2:p.Lys3267=
|
|
XM_011535203.1:c.9801G=
|
XP_011533505.1:p.Lys3267=
|
|
XM_011535204.1:c.9705G=
|
XP_011533506.1:p.Lys3235=
|
|
NM_000059.4:c.9801G=
MANE Select
|
NP_000050.3:p.Lys3267=
|
|