ENST00000327047.6:c.194T>G
MANE Select
|
ENSP00000322280.1:p.Leu65Arg
|
|
ENST00000468836.2:c.170T>G
|
ENSP00000419892.2:p.Leu57Arg
|
|
ENST00000644099.1:c.35T>G
|
ENSP00000494762.1:p.Leu12Arg
|
|
ENST00000645441.1:c.36T>G
|
|
|
ENST00000327047.5:c.194T>G
|
ENSP00000322280.1:p.Leu65Arg
|
|
ENST00000328863.8:c.194T>G
|
ENSP00000329158.4:p.Leu65Arg
|
|
ENST00000468836.1:c.-207T>G
|
ENSP00000419892.1:n.-207T>G
|
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ENST00000472224.1:n.200T>G
|
|
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NM_001195794.1:c.194T>G , LRG_700t1:c.194T>G
|
NP_001182723.1:p.Leu65Arg
|
|
NM_001256819.1:c.194T>G
|
NP_001243748.1:p.Leu65Arg
|
|
NM_174878.2:c.194T>G
|
NP_777367.1:p.Leu65Arg
|
|
NR_046380.2:n.485T>G
|
|
|
XR_924167.1:n.506T>G
|
|
|
NM_001256819.2:c.194T>G
|
NP_001243748.1:p.Leu65Arg
|
|
NM_174878.3:c.194T>G
MANE Select
|
NP_777367.1:p.Leu65Arg
|
|
NR_046380.3:n.213T>G
|
|
|