ENST00000463045.3:c.354A>T
|
ENSP00000481376.2:p.Glu118Asp
|
|
ENST00000491274.6:c.483A>T
|
ENSP00000480482.2:p.Glu161Asp
|
|
ENST00000375499.8:c.525A>T
MANE Select
|
ENSP00000364649.3:p.Glu175Asp
|
|
ENST00000375499.7:c.525A>T
|
ENSP00000364649.3:p.Glu175Asp
|
|
ENST00000463045.2:c.354A>T
|
ENSP00000481376.1:p.Glu118Asp
|
|
ENST00000475506.1:n.442A>T
|
|
|
ENST00000485515.5:n.459A>T
|
|
|
ENST00000491274.5:c.483A>T
|
ENSP00000480482.1:p.Glu161Asp
|
|
NM_003000.2:c.525A>T , LRG_316t1:c.525A>T
|
NP_002991.2:p.Glu175Asp
|
|
NM_003000.3:c.525A>T
MANE Select
|
NP_002991.2:p.Glu175Asp
|
|