ENST00000703783.1:n.1012G>C
|
|
|
ENST00000703785.1:n.1093G>C
|
|
|
ENST00000262464.9:c.4228G>C
MANE Select
|
ENSP00000262464.4:p.Asp1410His
|
|
ENST00000262464.8:c.4228G>C
|
ENSP00000262464.4:p.Asp1410His
|
|
ENST00000507835.5:c.778G>C
|
ENSP00000426839.1:p.Asp260His
|
|
ENST00000508053.5:c.4228G>C
|
ENSP00000424571.1:p.Asp1410His
|
|
ENST00000508989.5:c.4129G>C
|
ENSP00000425596.1:p.Asp1377His
|
|
ENST00000619499.4:c.4225G>C
|
ENSP00000482132.1:p.Asp1409His
|
|
NM_001999.3:c.4228G>C
|
NP_001990.2:p.Asp1410His
|
|
XM_017009228.2:c.4075G>C
|
XP_016864717.1:p.Asp1359His
|
|
NM_001999.4:c.4228G>C
MANE Select
|
NP_001990.2:p.Asp1410His
|
|