ENST00000327047.6:c.246G>T
MANE Select
|
ENSP00000322280.1:p.Arg82=
|
|
ENST00000468836.2:c.222G>T
|
ENSP00000419892.2:p.Arg74=
|
|
ENST00000644099.1:c.87G>T
|
ENSP00000494762.1:p.Arg29=
|
|
ENST00000645441.1:c.88G>T
|
|
|
ENST00000327047.5:c.246G>T
|
ENSP00000322280.1:p.Arg82=
|
|
ENST00000328863.8:c.246G>T
|
ENSP00000329158.4:p.Arg82=
|
|
ENST00000468836.1:c.-155G>T
|
ENSP00000419892.1:n.-155G>T
|
|
ENST00000472224.1:n.252G>T
|
|
|
NM_001195794.1:c.246G>T , LRG_700t1:c.246G>T
|
NP_001182723.1:p.Arg82=
|
|
NM_001256819.1:c.246G>T
|
NP_001243748.1:p.Arg82=
|
|
NM_174878.2:c.246G>T
|
NP_777367.1:p.Arg82=
|
|
NR_046380.2:n.537G>T
|
|
|
XR_924167.1:n.558G>T
|
|
|
NM_001256819.2:c.246G>T
|
NP_001243748.1:p.Arg82=
|
|
NM_174878.3:c.246G>T
MANE Select
|
NP_777367.1:p.Arg82=
|
|
NR_046380.3:n.265G>T
|
|
|