ENST00000470094.2:c.9305C>G
|
ENSP00000434898.2:p.Ala3102Gly
|
|
ENST00000528762.2:c.*672C>G
|
ENSP00000433168.2:n.*672C>G
|
|
ENST00000530893.7:c.8936C>G
|
ENSP00000499438.2:p.Ala2979Gly
|
|
ENST00000665585.2:c.*867C>G
|
ENSP00000499570.2:n.*867C>G
|
|
ENST00000666593.2:c.*150C>G
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ENSP00000499256.2:n.*150C>G
|
|
ENST00000700202.2:c.9254C>G
|
ENSP00000514856.2:p.Ala3085Gly
|
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ENST00000700202.1:c.1721C>G
|
ENSP00000514856.1:p.Ala574Gly
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ENST00000700203.1:n.1432C>G
|
|
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ENST00000380152.8:c.9305C>G
MANE Select
|
ENSP00000369497.3:p.Ala3102Gly
|
|
ENST00000544455.6:c.9305C>G
|
ENSP00000439902.1:p.Ala3102Gly
|
|
ENST00000614259.2:c.9313C>G
|
ENSP00000506251.1:n.9313C>G
|
|
ENST00000665585.1:c.2183C>G
|
|
|
ENST00000666593.1:c.327C>G
|
ENSP00000499256.1:n.327C>G
|
|
ENST00000680887.1:c.9305C>G
|
ENSP00000505508.1:p.Ala3102Gly
|
|
ENST00000380152.7:c.9305C>G
|
ENSP00000369497.3:p.Ala3102Gly
|
|
ENST00000470094.1:c.262C>G
|
|
|
ENST00000544455.5:c.9305C>G
|
ENSP00000439902.1:p.Ala3102Gly
|
|
NM_000059.3:c.9305C>G , LRG_293t1:c.9305C>G
|
NP_000050.2:p.Ala3102Gly
|
|
XM_011535203.1:c.9305C>G
|
XP_011533505.1:p.Ala3102Gly
|
|
XM_011535204.1:c.9209C>G
|
XP_011533506.1:p.Ala3070Gly
|
|
NM_000059.4:c.9305C>G
MANE Select
|
NP_000050.3:p.Ala3102Gly
|
|