ENST00000258385.8:c.1285C>T
MANE Select
|
ENSP00000258385.3:p.Gln429Ter
|
|
ENST00000258385.7:c.1285C>T
|
ENSP00000258385.3:p.Gln429Ter
|
|
ENST00000441621.6:c.*467C>T
|
ENSP00000408819.2:n.*467C>T
|
|
ENST00000446616.1:c.*926C>T
|
ENSP00000410801.1:n.*926C>T
|
|
ENST00000543200.5:c.1240C>T
|
ENSP00000438380.1:p.Gln414Ter
|
|
NM_000751.2:c.1285C>T
|
NP_000742.1:p.Gln429Ter
|
|
NM_001256657.1:c.1240C>T
|
NP_001243586.1:p.Gln414Ter
|
|
NM_001311195.1:c.703C>T
|
NP_001298124.1:p.Gln235Ter
|
|
NM_001311196.1:c.982C>T
|
NP_001298125.1:p.Gln328Ter
|
|
NR_046333.1:c.-4294966266C>T
|
|
|
NR_046334.1:c.-4294965987C>T
|
|
|
XM_011510524.1:c.904C>T
|
XP_011508826.1:p.Gln302Ter
|
|
XM_011510524.2:c.904C>T
|
XP_011508826.1:p.Gln302Ter
|
|
NM_000751.3:c.1285C>T
MANE Select
|
NP_000742.1:p.Gln429Ter
|
|
NM_001311195.2:c.703C>T
|
NP_001298124.1:p.Gln235Ter
|
|
NM_001311196.2:c.982C>T
|
NP_001298125.1:p.Gln328Ter
|
|
NM_001256657.2:c.1240C>T
|
NP_001243586.1:p.Gln414Ter
|
|