ENST00000327047.6:c.170T>A
MANE Select
|
ENSP00000322280.1:p.Phe57Tyr
|
|
ENST00000468836.2:c.146T>A
|
ENSP00000419892.2:p.Phe49Tyr
|
|
ENST00000644099.1:c.11T>A
|
ENSP00000494762.1:p.Phe4Tyr
|
|
ENST00000645441.1:c.12T>A
|
|
|
ENST00000327047.5:c.170T>A
|
ENSP00000322280.1:p.Phe57Tyr
|
|
ENST00000328863.8:c.170T>A
|
ENSP00000329158.4:p.Phe57Tyr
|
|
ENST00000468836.1:c.-231T>A
|
ENSP00000419892.1:n.-231T>A
|
|
ENST00000472224.1:n.176T>A
|
|
|
NM_001195794.1:c.170T>A , LRG_700t1:c.170T>A
|
NP_001182723.1:p.Phe57Tyr
|
|
NM_001256819.1:c.170T>A
|
NP_001243748.1:p.Phe57Tyr
|
|
NM_174878.2:c.170T>A
|
NP_777367.1:p.Phe57Tyr
|
|
NR_046380.2:n.461T>A
|
|
|
XR_924167.1:n.482T>A
|
|
|
NM_001256819.2:c.170T>A
|
NP_001243748.1:p.Phe57Tyr
|
|
NM_174878.3:c.170T>A
MANE Select
|
NP_777367.1:p.Phe57Tyr
|
|
NR_046380.3:n.189T>A
|
|
|