ENST00000258385.8:c.1252+11G>C
MANE Select
|
ENSP00000258385.3:n.1252+11G>C
|
|
ENST00000258385.7:c.1252+11G>C
|
ENSP00000258385.3:n.1252+11G>C
|
|
ENST00000441621.6:c.*434+11G>C
|
ENSP00000408819.2:n.*434+11G>C
|
|
ENST00000446616.1:c.*893+11G>C
|
ENSP00000410801.1:n.*893+11G>C
|
|
ENST00000543200.5:c.1207+11G>C
|
ENSP00000438380.1:n.1207+11G>C
|
|
NM_000751.2:c.1252+11G>C
|
NP_000742.1:n.1252+11G>C
|
|
NM_001256657.1:c.1207+11G>C
|
NP_001243586.1:n.1207+11G>C
|
|
NM_001311195.1:c.670+11G>C
|
NP_001298124.1:n.670+11G>C
|
|
NM_001311196.1:c.949+11G>C
|
NP_001298125.1:n.949+11G>C
|
|
NR_046333.1:c.-4294966299+11G>C
|
|
|
NR_046334.1:c.-4294966020+11G>C
|
|
|
XM_011510524.1:c.871+11G>C
|
XP_011508826.1:n.871+11G>C
|
|
XM_011510524.2:c.871+11G>C
|
XP_011508826.1:n.871+11G>C
|
|
NM_000751.3:c.1252+11G>C
MANE Select
|
NP_000742.1:n.1252+11G>C
|
|
NM_001311195.2:c.670+11G>C
|
NP_001298124.1:n.670+11G>C
|
|
NM_001311196.2:c.949+11G>C
|
NP_001298125.1:n.949+11G>C
|
|
NM_001256657.2:c.1207+11G>C
|
NP_001243586.1:n.1207+11G>C
|
|