ENST00000313468.10:c.341G>A
MANE Select
|
ENSP00000315774.5:p.Cys114Tyr
|
|
ENST00000313468.9:c.341G>A
|
ENSP00000315774.5:p.Cys114Tyr
|
|
ENST00000432321.6:n.458G>A
|
|
|
ENST00000453471.6:c.341G>A
|
ENSP00000403972.2:p.Cys114Tyr
|
|
ENST00000524810.5:c.112G>A
|
|
|
ENST00000525419.5:c.287G>A
|
ENSP00000433521.1:p.Cys96Tyr
|
|
ENST00000526339.5:c.341G>A
|
ENSP00000436287.1:p.Cys114Tyr
|
|
ENST00000526446.5:c.*396G>A
|
ENSP00000433645.1:n.*396G>A
|
|
ENST00000528492.1:c.-67+2519G>A
|
ENSP00000432848.1:n.-67+2519G>A
|
|
ENST00000529645.1:c.519G>A
|
ENSP00000431293.1:n.519G>A
|
|
ENST00000532399.1:n.1046G>A
|
|
|
NM_002496.3:c.341G>A
|
NP_002487.1:p.Cys114Tyr
|
|
XM_005274013.1:c.341G>A
|
XP_005274070.1:p.Cys114Tyr
|
|
XM_005274014.1:c.341G>A
|
XP_005274071.1:p.Cys114Tyr
|
|
XM_005274015.1:c.221G>A
|
XP_005274072.1:p.Cys74Tyr
|
|
XM_011545053.1:c.341G>A
|
XP_011543355.1:p.Cys114Tyr
|
|
NM_002496.4:c.341G>A
MANE Select
|
NP_002487.1:p.Cys114Tyr
|
|