ENST00000703783.1:n.671G>A
|
|
|
ENST00000703785.1:n.752G>A
|
|
|
ENST00000262464.9:c.3887G>A
MANE Select
|
ENSP00000262464.4:p.Gly1296Asp
|
|
ENST00000262464.8:c.3887G>A
|
ENSP00000262464.4:p.Gly1296Asp
|
|
ENST00000507835.5:c.437G>A
|
ENSP00000426839.1:p.Gly146Asp
|
|
ENST00000508053.5:c.3887G>A
|
ENSP00000424571.1:p.Gly1296Asp
|
|
ENST00000508989.5:c.3788G>A
|
ENSP00000425596.1:p.Gly1263Asp
|
|
ENST00000619499.4:c.3884G>A
|
ENSP00000482132.1:p.Gly1295Asp
|
|
NM_001999.3:c.3887G>A
|
NP_001990.2:p.Gly1296Asp
|
|
XM_017009228.2:c.3734G>A
|
XP_016864717.1:p.Gly1245Asp
|
|
NM_001999.4:c.3887G>A
MANE Select
|
NP_001990.2:p.Gly1296Asp
|
|