ENST00000428216.4:c.118G>T
MANE Select
|
ENSP00000401980.2:p.Asp40Tyr
|
|
ENST00000416600.6:c.-132+2894G>T
|
ENSP00000413749.2:n.-132+2894G>T
|
|
ENST00000428216.3:c.118G>T
|
ENSP00000401980.2:p.Asp40Tyr
|
|
NM_001206491.1:c.-132+2894G>T
|
NP_001193420.1:n.-132+2894G>T
|
|
NM_020746.4:c.118G>T
|
NP_065797.2:p.Asp40Tyr
|
|
NR_037921.1:n.290G>T
|
|
|
NM_020746.5:c.118G>T
MANE Select
|
NP_065797.2:p.Asp40Tyr
|
|
NR_037921.2:n.255G>T
|
|
|
NM_001206491.2:c.-132+2894G>T
|
NP_001193420.1:n.-132+2894G>T
|
|
NM_001385663.1:c.-430G>T
|
NP_001372592.1:n.-430G>T
|
|