ENST00000703783.1:n.382G>T
|
|
|
ENST00000703785.1:n.463G>T
|
|
|
ENST00000262464.9:c.3598G>T
MANE Select
|
ENSP00000262464.4:p.Asp1200Tyr
|
|
ENST00000262464.8:c.3598G>T
|
ENSP00000262464.4:p.Asp1200Tyr
|
|
ENST00000507835.5:c.148G>T
|
ENSP00000426839.1:p.Asp50Tyr
|
|
ENST00000508053.5:c.3598G>T
|
ENSP00000424571.1:p.Asp1200Tyr
|
|
ENST00000508989.5:c.3499G>T
|
ENSP00000425596.1:p.Asp1167Tyr
|
|
ENST00000619499.4:c.3595G>T
|
ENSP00000482132.1:p.Asp1199Tyr
|
|
NM_001999.3:c.3598G>T
|
NP_001990.2:p.Asp1200Tyr
|
|
XM_017009228.2:c.3445G>T
|
XP_016864717.1:p.Asp1149Tyr
|
|
NM_001999.4:c.3598G>T
MANE Select
|
NP_001990.2:p.Asp1200Tyr
|
|