ENST00000307998.11:c.932A>T
MANE Select
|
ENSP00000309953.6:p.Asp311Val
|
|
ENST00000307998.10:c.932A>T
|
ENSP00000309953.6:p.Asp311Val
|
|
ENST00000525392.1:n.93A>T
|
|
|
ENST00000526628.5:n.1498A>T
|
|
|
ENST00000528176.5:c.932A>T
|
ENSP00000434151.1:p.Asp311Val
|
|
ENST00000528409.1:n.176A>T
|
|
|
ENST00000530806.5:c.-67A>T
|
ENSP00000436526.1:n.-67A>T
|
|
ENST00000531005.5:n.1926A>T
|
|
|
ENST00000531645.5:c.80A>T
|
ENSP00000436521.1:p.Asp27Val
|
|
ENST00000531972.5:c.932A>T
|
ENSP00000435295.1:p.Asp311Val
|
|
ENST00000532084.5:n.358A>T
|
|
|
NM_016938.4:c.932A>T
|
NP_058634.4:p.Asp311Val
|
|
NR_037718.1:n.1191A>T
|
|
|
NM_016938.5:c.932A>T
MANE Select
|
NP_058634.4:p.Asp311Val
|
|
NR_037718.2:n.1057A>T
|
|
|