ENST00000327047.6:c.230G>T
MANE Select
|
ENSP00000322280.1:p.Gly77Val
|
|
ENST00000468836.2:c.206G>T
|
ENSP00000419892.2:p.Gly69Val
|
|
ENST00000644099.1:c.71G>T
|
ENSP00000494762.1:p.Gly24Val
|
|
ENST00000645441.1:c.72G>T
|
|
|
ENST00000327047.5:c.230G>T
|
ENSP00000322280.1:p.Gly77Val
|
|
ENST00000328863.8:c.230G>T
|
ENSP00000329158.4:p.Gly77Val
|
|
ENST00000468836.1:c.-171G>T
|
ENSP00000419892.1:n.-171G>T
|
|
ENST00000472224.1:n.236G>T
|
|
|
NM_001195794.1:c.230G>T , LRG_700t1:c.230G>T
|
NP_001182723.1:p.Gly77Val
|
|
NM_001256819.1:c.230G>T
|
NP_001243748.1:p.Gly77Val
|
|
NM_174878.2:c.230G>T
|
NP_777367.1:p.Gly77Val
|
|
NR_046380.2:n.521G>T
|
|
|
XR_924167.1:n.542G>T
|
|
|
NM_001256819.2:c.230G>T
|
NP_001243748.1:p.Gly77Val
|
|
NM_174878.3:c.230G>T
MANE Select
|
NP_777367.1:p.Gly77Val
|
|
NR_046380.3:n.249G>T
|
|
|