ENST00000327047.6:c.125C>G
MANE Select
|
ENSP00000322280.1:p.Thr42Arg
|
|
ENST00000468836.2:c.101C>G
|
ENSP00000419892.2:p.Thr34Arg
|
|
ENST00000327047.5:c.125C>G
|
ENSP00000322280.1:p.Thr42Arg
|
|
ENST00000328863.8:c.125C>G
|
ENSP00000329158.4:p.Thr42Arg
|
|
ENST00000468836.1:c.-276C>G
|
ENSP00000419892.1:n.-276C>G
|
|
ENST00000472224.1:n.131C>G
|
|
|
NM_001195794.1:c.125C>G , LRG_700t1:c.125C>G
|
NP_001182723.1:p.Thr42Arg
|
|
NM_001256819.1:c.125C>G
|
NP_001243748.1:p.Thr42Arg
|
|
NM_174878.2:c.125C>G
|
NP_777367.1:p.Thr42Arg
|
|
NR_046380.2:n.416C>G
|
|
|
XR_924167.1:n.437C>G
|
|
|
NM_001256819.2:c.125C>G
|
NP_001243748.1:p.Thr42Arg
|
|
NM_174878.3:c.125C>G
MANE Select
|
NP_777367.1:p.Thr42Arg
|
|
NR_046380.3:n.144C>G
|
|
|