ENST00000703783.1:n.680G>A
|
|
|
ENST00000703785.1:n.761G>A
|
|
|
ENST00000262464.9:c.3896G>A
MANE Select
|
ENSP00000262464.4:p.Cys1299Tyr
|
|
ENST00000262464.8:c.3896G>A
|
ENSP00000262464.4:p.Cys1299Tyr
|
|
ENST00000507835.5:c.446G>A
|
ENSP00000426839.1:p.Cys149Tyr
|
|
ENST00000508053.5:c.3896G>A
|
ENSP00000424571.1:p.Cys1299Tyr
|
|
ENST00000508989.5:c.3797G>A
|
ENSP00000425596.1:p.Cys1266Tyr
|
|
ENST00000619499.4:c.3893G>A
|
ENSP00000482132.1:p.Cys1298Tyr
|
|
NM_001999.3:c.3896G>A
|
NP_001990.2:p.Cys1299Tyr
|
|
XM_017009228.2:c.3743G>A
|
XP_016864717.1:p.Cys1248Tyr
|
|
NM_001999.4:c.3896G>A
MANE Select
|
NP_001990.2:p.Cys1299Tyr
|
|