ENST00000321612.8:c.2007G>T
MANE Select
|
ENSP00000370737.4:p.Glu669Asp
|
|
ENST00000460457.2:n.167G>T
|
|
|
ENST00000638233.1:n.442G>T
|
|
|
ENST00000638661.1:c.207G>T
|
ENSP00000491369.1:p.Glu69Asp
|
|
ENST00000638694.1:n.194G>T
|
|
|
ENST00000639318.1:c.207G>T
|
ENSP00000491932.1:p.Glu69Asp
|
|
ENST00000639364.1:n.1707G>T
|
|
|
ENST00000639443.1:n.1575G>T
|
|
|
ENST00000639954.1:n.1715G>T
|
|
|
ENST00000640208.1:c.207G>T
|
ENSP00000491895.1:p.Glu69Asp
|
|
ENST00000640505.1:n.246G>T
|
|
|
ENST00000640592.1:n.1890G>T
|
|
|
ENST00000321612.6:c.2007G>T
|
ENSP00000370737.3:p.Glu669Asp
|
|
ENST00000460457.1:n.146G>T
|
|
|
NM_000170.2:c.2007G>T , LRG_643t1:c.2007G>T
|
NP_000161.2:p.Glu669Asp
|
|
NM_000170.3:c.2007G>T
MANE Select
|
NP_000161.2:p.Glu669Asp
|
|