ENST00000360228.11:c.564G>T
MANE Select
|
ENSP00000353362.5:p.Glu188Asp
|
|
ENST00000573710.7:c.564G>T
|
ENSP00000460092.3:p.Glu188Asp
|
|
ENST00000593160.2:n.279G>T
|
|
|
ENST00000635727.1:c.564G>T
|
ENSP00000490001.1:p.Glu188Asp
|
|
ENST00000635895.1:c.564G>T
|
ENSP00000490323.1:p.Glu188Asp
|
|
ENST00000636012.1:c.564G>T
|
ENSP00000490223.1:p.Glu188Asp
|
|
ENST00000636389.1:c.564G>T
|
ENSP00000489992.1:p.Glu188Asp
|
|
ENST00000636549.1:c.564G>T
|
ENSP00000490578.1:p.Glu188Asp
|
|
ENST00000636966.1:n.452G>T
|
|
|
ENST00000637276.1:c.564G>T
|
ENSP00000489777.1:p.Glu188Asp
|
|
ENST00000637432.1:c.564G>T
|
ENSP00000490617.1:p.Glu188Asp
|
|
ENST00000637736.1:c.423G>T
|
ENSP00000489861.1:p.Glu141Asp
|
|
ENST00000637769.1:c.564G>T
|
ENSP00000489778.1:p.Glu188Asp
|
|
ENST00000637927.1:c.564G>T
|
ENSP00000489715.1:p.Glu188Asp
|
|
ENST00000637966.1:n.417G>T
|
|
|
ENST00000637981.1:n.382G>T
|
|
|
ENST00000638009.2:c.564G>T
|
ENSP00000489913.1:p.Glu188Asp
|
|
ENST00000638029.1:c.564G>T
|
ENSP00000489829.1:p.Glu188Asp
|
|
ENST00000664864.1:c.759G>T
|
ENSP00000499449.1:p.Glu253Asp
|
|
ENST00000360228.9:c.564G>T
|
ENSP00000353362.5:p.Glu188Asp
|
|
ENST00000573710.6:c.564G>T
|
ENSP00000460092.2:p.Glu188Asp
|
|
ENST00000614285.4:c.564G>T
|
ENSP00000479983.1:p.Glu188Asp
|
|
NM_000068.3:c.564G>T
|
NP_000059.3:p.Glu188Asp
|
|
NM_001127221.1:c.564G>T , LRG_7t1:c.564G>T
|
NP_001120693.1:p.Glu188Asp
|
|
NM_001127222.1:c.564G>T
|
NP_001120694.1:p.Glu188Asp
|
|
NM_001174080.1:c.564G>T
|
NP_001167551.1:p.Glu188Asp
|
|
NM_023035.2:c.564G>T
|
NP_075461.2:p.Glu188Asp
|
|
NM_000068.4:c.564G>T
|
NP_000059.3:p.Glu188Asp
|
|
NM_001127222.2:c.564G>T
MANE Select
|
NP_001120694.1:p.Glu188Asp
|
|
NM_001174080.2:c.564G>T
|
NP_001167551.1:p.Glu188Asp
|
|
NM_023035.3:c.564G>T
|
NP_075461.2:p.Glu188Asp
|
|
NM_001127221.2:c.564G>T
|
NP_001120693.1:p.Glu188Asp
|
|