ENST00000470094.2:c.*260C>G
|
ENSP00000434898.2:n.*260C>G
|
|
ENST00000528762.2:c.*1104C>G
|
ENSP00000433168.2:n.*1104C>G
|
|
ENST00000530893.7:c.9368C>G
|
ENSP00000499438.2:p.Ala3123Gly
|
|
ENST00000665585.2:c.*1299C>G
|
ENSP00000499570.2:n.*1299C>G
|
|
ENST00000700202.2:c.9686C>G
|
ENSP00000514856.2:p.Ala3229Gly
|
|
ENST00000700202.1:c.2153C>G
|
ENSP00000514856.1:p.Ala718Gly
|
|
ENST00000700203.1:n.1864C>G
|
|
|
ENST00000380152.8:c.9737C>G
MANE Select
|
ENSP00000369497.3:p.Ala3246Gly
|
|
ENST00000544455.6:c.9737C>G
|
ENSP00000439902.1:p.Ala3246Gly
|
|
ENST00000614259.2:c.9745C>G
|
ENSP00000506251.1:n.9745C>G
|
|
ENST00000680887.1:c.9737C>G
|
ENSP00000505508.1:p.Ala3246Gly
|
|
ENST00000380152.7:c.9737C>G
|
ENSP00000369497.3:p.Ala3246Gly
|
|
ENST00000470094.1:c.820C>G
|
|
|
ENST00000533776.1:n.325C>G
|
|
|
ENST00000544455.5:c.9737C>G
|
ENSP00000439902.1:p.Ala3246Gly
|
|
NM_000059.3:c.9737C>G , LRG_293t1:c.9737C>G
|
NP_000050.2:p.Ala3246Gly
|
|
XM_011535203.1:c.9737C>G
|
XP_011533505.1:p.Ala3246Gly
|
|
XM_011535204.1:c.9641C>G
|
XP_011533506.1:p.Ala3214Gly
|
|
NM_000059.4:c.9737C>G
MANE Select
|
NP_000050.3:p.Ala3246Gly
|
|