ENST00000349748.8:c.1265A>G
|
ENSP00000183936.4:p.Asp422Gly
|
|
ENST00000357568.8:c.1409A>G
|
ENSP00000350181.3:p.Asp470Gly
|
|
ENST00000397163.8:c.1409A>G
MANE Select
|
ENSP00000380349.3:p.Asp470Gly
|
|
ENST00000466369.5:n.1918A>G
|
|
|
ENST00000483208.5:n.1640A>G
|
|
|
ENST00000495723.1:n.1640A>G
|
|
|
ENST00000549793.5:n.1640A>G
|
|
|
ENST00000638141.2:n.1280A>G
|
|
|
ENST00000673705.1:c.309+2043A>G
|
ENSP00000501021.1:n.309+2043A>G
|
|
ENST00000318023.11:c.1265A>G
|
ENSP00000326281.8:p.Asp422Gly
|
|
ENST00000349748.7:c.1265A>G
|
ENSP00000183936.4:p.Asp422Gly
|
|
ENST00000357568.7:c.1409A>G
|
ENSP00000350181.3:p.Asp470Gly
|
|
ENST00000397163.7:c.1409A>G
|
ENSP00000380349.3:p.Asp470Gly
|
|
NM_000070.2:c.1409A>G
|
NP_000061.1:p.Asp470Gly
|
|
NM_024344.1:c.1409A>G
|
NP_077320.1:p.Asp470Gly
|
|
NM_173087.1:c.1265A>G
|
NP_775110.1:p.Asp422Gly
|
|
NM_000070.3:c.1409A>G
MANE Select
|
NP_000061.1:p.Asp470Gly
|
|
NM_024344.2:c.1409A>G
|
NP_077320.1:p.Asp470Gly
|
|
NM_173087.2:c.1265A>G
|
NP_775110.1:p.Asp422Gly
|
|