ENST00000703783.1:n.517G>T
|
|
|
ENST00000703785.1:n.598G>T
|
|
|
ENST00000262464.9:c.3733G>T
MANE Select
|
ENSP00000262464.4:p.Glu1245Ter
|
|
ENST00000262464.8:c.3733G>T
|
ENSP00000262464.4:p.Glu1245Ter
|
|
ENST00000507835.5:c.283G>T
|
ENSP00000426839.1:p.Glu95Ter
|
|
ENST00000508053.5:c.3733G>T
|
ENSP00000424571.1:p.Glu1245Ter
|
|
ENST00000508989.5:c.3634G>T
|
ENSP00000425596.1:p.Glu1212Ter
|
|
ENST00000619499.4:c.3730G>T
|
ENSP00000482132.1:p.Glu1244Ter
|
|
NM_001999.3:c.3733G>T
|
NP_001990.2:p.Glu1245Ter
|
|
XM_017009228.2:c.3580G>T
|
XP_016864717.1:p.Glu1194Ter
|
|
NM_001999.4:c.3733G>T
MANE Select
|
NP_001990.2:p.Glu1245Ter
|
|