ENST00000527168.6:n.747T>G
|
|
|
ENST00000529110.2:c.732T>G
|
ENSP00000435349.2:p.Ala244=
|
|
ENST00000529957.6:n.706T>G
|
|
|
ENST00000683366.1:c.*380T>G
|
ENSP00000507283.1:n.*380T>G
|
|
ENST00000683887.1:c.696T>G
|
ENSP00000506886.1:p.Ala232=
|
|
ENST00000684100.1:n.642T>G
|
|
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ENST00000684126.1:n.782T>G
|
|
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ENST00000684688.1:n.1273T>G
|
|
|
ENST00000204679.9:c.648T>G
MANE Select
|
ENSP00000204679.4:p.Ala216=
|
|
ENST00000204679.8:c.648T>G
|
ENSP00000204679.4:p.Ala216=
|
|
ENST00000527076.1:n.1871T>G
|
|
|
ENST00000527168.5:n.815T>G
|
|
|
ENST00000529957.5:n.747T>G
|
|
|
NM_032520.4:c.648T>G
|
NP_115909.1:p.Ala216=
|
|
XM_017023782.1:c.696T>G
|
XP_016879271.1:p.Ala232=
|
|
XM_017023783.1:c.288T>G
|
XP_016879272.1:p.Ala96=
|
|
NM_032520.5:c.648T>G
MANE Select
|
NP_115909.1:p.Ala216=
|
|