ENST00000262367.10:c.5423G>A
MANE Select
|
ENSP00000262367.5:p.Cys1808Tyr
|
|
ENST00000262367.9:c.5423G>A
|
ENSP00000262367.5:p.Cys1808Tyr
|
|
ENST00000382070.7:c.5309G>A
|
ENSP00000371502.3:p.Cys1770Tyr
|
|
NM_001079846.1:c.5309G>A
|
NP_001073315.1:p.Cys1770Tyr
|
|
NM_004380.2:c.5423G>A
|
NP_004371.2:p.Cys1808Tyr
|
|
XM_005255124.3:c.5378G>A
|
XP_005255181.1:p.Cys1793Tyr
|
|
XM_005255125.3:c.5006G>A
|
XP_005255182.1:p.Cys1669Tyr
|
|
XM_006720848.2:c.5162G>A
|
XP_006720911.1:p.Cys1721Tyr
|
|
XM_011522380.1:c.5369G>A
|
XP_011520682.1:p.Cys1790Tyr
|
|
XM_011522381.1:c.4670G>A
|
XP_011520683.1:p.Cys1557Tyr
|
|
XM_005255124.4:c.5378G>A
|
XP_005255181.1:p.Cys1793Tyr
|
|
XM_005255125.4:c.5006G>A
|
XP_005255182.1:p.Cys1669Tyr
|
|
XM_006720848.3:c.5162G>A
|
XP_006720911.1:p.Cys1721Tyr
|
|
XM_011522381.2:c.4670G>A
|
XP_011520683.1:p.Cys1557Tyr
|
|
XM_017022944.1:c.5417G>A
|
XP_016878433.1:p.Cys1806Tyr
|
|
NM_004380.3:c.5423G>A
MANE Select
|
NP_004371.2:p.Cys1808Tyr
|
|