ENST00000470094.2:c.*447C>A
|
ENSP00000434898.2:n.*447C>A
|
|
ENST00000528762.2:c.*1291C>A
|
ENSP00000433168.2:n.*1291C>A
|
|
ENST00000530893.7:c.9555C>A
|
ENSP00000499438.2:p.Tyr3185Ter
|
|
ENST00000665585.2:c.*1486C>A
|
ENSP00000499570.2:n.*1486C>A
|
|
ENST00000700202.2:c.9873C>A
|
ENSP00000514856.2:p.Tyr3291Ter
|
|
ENST00000700202.1:c.2340C>A
|
ENSP00000514856.1:p.Tyr780Ter
|
|
ENST00000700203.1:n.2051C>A
|
|
|
ENST00000380152.8:c.9924C>A
MANE Select
|
ENSP00000369497.3:p.Tyr3308Ter
|
|
ENST00000544455.6:c.9924C>A
|
ENSP00000439902.1:p.Tyr3308Ter
|
|
ENST00000614259.2:c.9932C>A
|
ENSP00000506251.1:n.9932C>A
|
|
ENST00000680887.1:c.9924C>A
|
ENSP00000505508.1:p.Tyr3308Ter
|
|
ENST00000380152.7:c.9924C>A
|
ENSP00000369497.3:p.Tyr3308Ter
|
|
ENST00000533776.1:n.512C>A
|
|
|
ENST00000544455.5:c.9924C>A
|
ENSP00000439902.1:p.Tyr3308Ter
|
|
NM_000059.3:c.9924C>A , LRG_293t1:c.9924C>A
|
NP_000050.2:p.Tyr3308Ter
|
|
XM_011535203.1:c.9924C>A
|
XP_011533505.1:p.Tyr3308Ter
|
|
XM_011535204.1:c.9828C>A
|
XP_011533506.1:p.Tyr3276Ter
|
|
NM_000059.4:c.9924C>A
MANE Select
|
NP_000050.3:p.Tyr3308Ter
|
|