ENST00000463045.3:c.353A>T
|
ENSP00000481376.2:p.Glu118Val
|
|
ENST00000491274.6:c.482A>T
|
ENSP00000480482.2:p.Glu161Val
|
|
ENST00000375499.8:c.524A>T
MANE Select
|
ENSP00000364649.3:p.Glu175Val
|
|
ENST00000375499.7:c.524A>T
|
ENSP00000364649.3:p.Glu175Val
|
|
ENST00000463045.2:c.353A>T
|
ENSP00000481376.1:p.Glu118Val
|
|
ENST00000475506.1:n.441A>T
|
|
|
ENST00000485515.5:n.458A>T
|
|
|
ENST00000491274.5:c.482A>T
|
ENSP00000480482.1:p.Glu161Val
|
|
NM_003000.2:c.524A>T , LRG_316t1:c.524A>T
|
NP_002991.2:p.Glu175Val
|
|
NM_003000.3:c.524A>T
MANE Select
|
NP_002991.2:p.Glu175Val
|
|