ENST00000470094.2:c.*279T>G
|
ENSP00000434898.2:n.*279T>G
|
|
ENST00000528762.2:c.*1123T>G
|
ENSP00000433168.2:n.*1123T>G
|
|
ENST00000530893.7:c.9387T>G
|
ENSP00000499438.2:p.Ser3129=
|
|
ENST00000665585.2:c.*1318T>G
|
ENSP00000499570.2:n.*1318T>G
|
|
ENST00000700202.2:c.9705T>G
|
ENSP00000514856.2:p.Ser3235=
|
|
ENST00000700202.1:c.2172T>G
|
ENSP00000514856.1:p.Ser724=
|
|
ENST00000700203.1:n.1883T>G
|
|
|
ENST00000380152.8:c.9756T>G
MANE Select
|
ENSP00000369497.3:p.Ser3252=
|
|
ENST00000544455.6:c.9756T>G
|
ENSP00000439902.1:p.Ser3252=
|
|
ENST00000614259.2:c.9764T>G
|
ENSP00000506251.1:n.9764T>G
|
|
ENST00000680887.1:c.9756T>G
|
ENSP00000505508.1:p.Ser3252=
|
|
ENST00000380152.7:c.9756T>G
|
ENSP00000369497.3:p.Ser3252=
|
|
ENST00000470094.1:c.839T>G
|
|
|
ENST00000533776.1:n.344T>G
|
|
|
ENST00000544455.5:c.9756T>G
|
ENSP00000439902.1:p.Ser3252=
|
|
NM_000059.3:c.9756T>G , LRG_293t1:c.9756T>G
|
NP_000050.2:p.Ser3252=
|
|
XM_011535203.1:c.9756T>G
|
XP_011533505.1:p.Ser3252=
|
|
XM_011535204.1:c.9660T>G
|
XP_011533506.1:p.Ser3220=
|
|
NM_000059.4:c.9756T>G
MANE Select
|
NP_000050.3:p.Ser3252=
|
|