ENST00000703783.1:n.1022C>A
|
|
|
ENST00000703785.1:n.1103C>A
|
|
|
ENST00000262464.9:c.4238C>A
MANE Select
|
ENSP00000262464.4:p.Ser1413Tyr
|
|
ENST00000262464.8:c.4238C>A
|
ENSP00000262464.4:p.Ser1413Tyr
|
|
ENST00000507835.5:c.788C>A
|
ENSP00000426839.1:p.Ser263Tyr
|
|
ENST00000508053.5:c.4238C>A
|
ENSP00000424571.1:p.Ser1413Tyr
|
|
ENST00000508989.5:c.4139C>A
|
ENSP00000425596.1:p.Ser1380Tyr
|
|
ENST00000619499.4:c.4235C>A
|
ENSP00000482132.1:p.Ser1412Tyr
|
|
NM_001999.3:c.4238C>A
|
NP_001990.2:p.Ser1413Tyr
|
|
XM_017009228.2:c.4085C>A
|
XP_016864717.1:p.Ser1362Tyr
|
|
NM_001999.4:c.4238C>A
MANE Select
|
NP_001990.2:p.Ser1413Tyr
|
|