ENST00000205402.10:c.1457C>T
MANE Select
|
ENSP00000205402.3:p.Ala486Val
|
|
ENST00000205402.9:c.1457C>T
|
ENSP00000205402.3:p.Ala486Val
|
|
ENST00000415325.5:c.*1131C>T
|
ENSP00000402593.1:n.*1131C>T
|
|
ENST00000417551.5:c.1457C>T
|
ENSP00000390667.1:p.Ala486Val
|
|
ENST00000437604.6:c.1313C>T
|
ENSP00000387542.2:p.Ala438Val
|
|
ENST00000440410.5:c.1388C>T
|
ENSP00000417016.1:p.Ala463Val
|
|
NM_000108.4:c.1457C>T
|
NP_000099.2:p.Ala486Val
|
|
NM_001289750.1:c.1160C>T
|
NP_001276679.1:p.Ala387Val
|
|
NM_001289751.1:c.1388C>T
|
NP_001276680.1:p.Ala463Val
|
|
NM_001289752.1:c.1313C>T
|
NP_001276681.1:p.Ala438Val
|
|
NM_000108.5:c.1457C>T
MANE Select
|
NP_000099.2:p.Ala486Val
|
|