ENST00000703783.1:n.375C>A
|
|
|
ENST00000703785.1:n.456C>A
|
|
|
ENST00000262464.9:c.3591C>A
MANE Select
|
ENSP00000262464.4:p.Asp1197Glu
|
|
ENST00000262464.8:c.3591C>A
|
ENSP00000262464.4:p.Asp1197Glu
|
|
ENST00000507835.5:c.141C>A
|
ENSP00000426839.1:p.Asp47Glu
|
|
ENST00000508053.5:c.3591C>A
|
ENSP00000424571.1:p.Asp1197Glu
|
|
ENST00000508989.5:c.3492C>A
|
ENSP00000425596.1:p.Asp1164Glu
|
|
ENST00000619499.4:c.3588C>A
|
ENSP00000482132.1:p.Asp1196Glu
|
|
NM_001999.3:c.3591C>A
|
NP_001990.2:p.Asp1197Glu
|
|
XM_017009228.2:c.3438C>A
|
XP_016864717.1:p.Asp1146Glu
|
|
NM_001999.4:c.3591C>A
MANE Select
|
NP_001990.2:p.Asp1197Glu
|
|