ENST00000262367.10:c.6132C>A
MANE Select
|
ENSP00000262367.5:p.Ala2044=
|
|
ENST00000262367.9:c.6132C>A
|
ENSP00000262367.5:p.Ala2044=
|
|
ENST00000382070.7:c.6018C>A
|
ENSP00000371502.3:p.Ala2006=
|
|
NM_001079846.1:c.6018C>A
|
NP_001073315.1:p.Ala2006=
|
|
NM_004380.2:c.6132C>A
|
NP_004371.2:p.Ala2044=
|
|
XM_005255124.3:c.6087C>A
|
XP_005255181.1:p.Ala2029=
|
|
XM_005255125.3:c.5715C>A
|
XP_005255182.1:p.Ala1905=
|
|
XM_006720848.2:c.5871C>A
|
XP_006720911.1:p.Ala1957=
|
|
XM_011522380.1:c.6078C>A
|
XP_011520682.1:p.Ala2026=
|
|
XM_011522381.1:c.5379C>A
|
XP_011520683.1:p.Ala1793=
|
|
XM_005255124.4:c.6087C>A
|
XP_005255181.1:p.Ala2029=
|
|
XM_005255125.4:c.5715C>A
|
XP_005255182.1:p.Ala1905=
|
|
XM_006720848.3:c.5871C>A
|
XP_006720911.1:p.Ala1957=
|
|
XM_011522381.2:c.5379C>A
|
XP_011520683.1:p.Ala1793=
|
|
XM_017022944.1:c.6126C>A
|
XP_016878433.1:p.Ala2042=
|
|
NM_004380.3:c.6132C>A
MANE Select
|
NP_004371.2:p.Ala2044=
|
|