|
NM_004380.3:c.5638C>T
MANE Select
|
NP_004371.2:p.Gln1880Ter
|
|
ENST00000262367.10:c.5638C>T
MANE Select
|
ENSP00000262367.5:p.Gln1880Ter
|
|
NM_001079846.1:c.5524C>T
|
NP_001073315.1:p.Gln1842Ter
|
|
NM_004380.2:c.5638C>T
|
NP_004371.2:p.Gln1880Ter
|
|
ENST00000262367.9:c.5638C>T
|
ENSP00000262367.5:p.Gln1880Ter
|
|
ENST00000382070.7:c.5524C>T
|
ENSP00000371502.3:p.Gln1842Ter
|
|
XM_005255124.3:c.5593C>T
|
XP_005255181.1:p.Gln1865Ter
|
|
XM_005255124.4:c.5593C>T
|
XP_005255181.1:p.Gln1865Ter
|
|
XM_005255125.3:c.5221C>T
|
XP_005255182.1:p.Gln1741Ter
|
|
XM_005255125.4:c.5221C>T
|
XP_005255182.1:p.Gln1741Ter
|
|
XM_006720848.2:c.5377C>T
|
XP_006720911.1:p.Gln1793Ter
|
|
XM_006720848.3:c.5377C>T
|
XP_006720911.1:p.Gln1793Ter
|
|
XM_011522380.1:c.5584C>T
|
XP_011520682.1:p.Gln1862Ter
|
|
XM_011522381.1:c.4885C>T
|
XP_011520683.1:p.Gln1629Ter
|
|
XM_011522381.2:c.4885C>T
|
XP_011520683.1:p.Gln1629Ter
|
|
XM_017022944.1:c.5632C>T
|
XP_016878433.1:p.Gln1878Ter
|