ENST00000254722.9:c.295C>T
MANE Select
|
ENSP00000254722.4:p.Arg99Ter
|
|
ENST00000254722.8:c.295C>T
|
ENSP00000254722.4:p.Arg99Ter
|
|
ENST00000570731.5:c.295C>T
|
ENSP00000459869.1:p.Arg99Ter
|
|
ENST00000570820.1:n.515C>T
|
|
|
ENST00000571360.5:c.256C>T
|
ENSP00000461660.1:p.Arg86Ter
|
|
ENST00000571870.5:n.536C>T
|
|
|
ENST00000573770.5:c.*145C>T
|
ENSP00000459107.1:n.*145C>T
|
|
ENST00000576406.5:c.-267C>T
|
ENSP00000461214.1:n.-267C>T
|
|
ENST00000577053.1:c.295C>T
|
ENSP00000460842.1:p.Arg99Ter
|
|
NM_002615.5:c.295C>T
|
NP_002606.3:p.Arg99Ter
|
|
NM_001329903.1:c.295C>T
|
NP_001316832.1:p.Arg99Ter
|
|
NM_001329904.1:c.-267C>T
|
NP_001316833.1:n.-267C>T
|
|
NM_002615.6:c.295C>T
|
NP_002606.3:p.Arg99Ter
|
|
NM_002615.7:c.295C>T
MANE Select
|
NP_002606.3:p.Arg99Ter
|
|
NM_001329903.2:c.295C>T
|
NP_001316832.1:p.Arg99Ter
|
|
NM_001329904.2:c.-267C>T
|
NP_001316833.1:n.-267C>T
|
|