ENST00000262367.10:c.6318C>A
MANE Select
|
ENSP00000262367.5:p.Ala2106=
|
|
ENST00000262367.9:c.6318C>A
|
ENSP00000262367.5:p.Ala2106=
|
|
ENST00000382070.7:c.6204C>A
|
ENSP00000371502.3:p.Ala2068=
|
|
NM_001079846.1:c.6204C>A
|
NP_001073315.1:p.Ala2068=
|
|
NM_004380.2:c.6318C>A
|
NP_004371.2:p.Ala2106=
|
|
XM_005255124.3:c.6273C>A
|
XP_005255181.1:p.Ala2091=
|
|
XM_005255125.3:c.5901C>A
|
XP_005255182.1:p.Ala1967=
|
|
XM_006720848.2:c.6057C>A
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XP_006720911.1:p.Ala2019=
|
|
XM_011522380.1:c.6264C>A
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XP_011520682.1:p.Ala2088=
|
|
XM_011522381.1:c.5565C>A
|
XP_011520683.1:p.Ala1855=
|
|
XM_005255124.4:c.6273C>A
|
XP_005255181.1:p.Ala2091=
|
|
XM_005255125.4:c.5901C>A
|
XP_005255182.1:p.Ala1967=
|
|
XM_006720848.3:c.6057C>A
|
XP_006720911.1:p.Ala2019=
|
|
XM_011522381.2:c.5565C>A
|
XP_011520683.1:p.Ala1855=
|
|
XM_017022944.1:c.6312C>A
|
XP_016878433.1:p.Ala2104=
|
|
NM_004380.3:c.6318C>A
MANE Select
|
NP_004371.2:p.Ala2106=
|
|