ENST00000327047.6:c.237G>C
MANE Select
|
ENSP00000322280.1:p.Arg79Ser
|
|
ENST00000468836.2:c.213G>C
|
ENSP00000419892.2:p.Arg71Ser
|
|
ENST00000644099.1:c.78G>C
|
ENSP00000494762.1:p.Arg26Ser
|
|
ENST00000645441.1:c.79G>C
|
|
|
ENST00000327047.5:c.237G>C
|
ENSP00000322280.1:p.Arg79Ser
|
|
ENST00000328863.8:c.237G>C
|
ENSP00000329158.4:p.Arg79Ser
|
|
ENST00000468836.1:c.-164G>C
|
ENSP00000419892.1:n.-164G>C
|
|
ENST00000472224.1:n.243G>C
|
|
|
NM_001195794.1:c.237G>C , LRG_700t1:c.237G>C
|
NP_001182723.1:p.Arg79Ser
|
|
NM_001256819.1:c.237G>C
|
NP_001243748.1:p.Arg79Ser
|
|
NM_174878.2:c.237G>C
|
NP_777367.1:p.Arg79Ser
|
|
NR_046380.2:n.528G>C
|
|
|
XR_924167.1:n.549G>C
|
|
|
NM_001256819.2:c.237G>C
|
NP_001243748.1:p.Arg79Ser
|
|
NM_174878.3:c.237G>C
MANE Select
|
NP_777367.1:p.Arg79Ser
|
|
NR_046380.3:n.256G>C
|
|
|