ENST00000245923.9:c.1139C>G
(RTN2)
MANE Select
|
ENSP00000245923.3:p.Ala380Gly
|
|
ENST00000245923.8:c.1139C>G
(RTN2)
|
ENSP00000245923.3:p.Ala380Gly
|
|
ENST00000344680.8:c.920C>G
(RTN2)
|
ENSP00000345127.3:p.Ala307Gly
|
|
ENST00000401705.5:c.-16+469G>C
(PPM1N)
|
ENSP00000384318.1:n.-16+469G>C
|
|
ENST00000430715.6:c.119C>G
(RTN2)
|
ENSP00000398178.1:p.Ala40Gly
|
|
ENST00000587597.5:c.1139C>G
(RTN2)
|
ENSP00000468144.1:p.Ala380Gly
|
|
ENST00000588036.5:n.80-462C>G
(RTN2)
|
|
|
ENST00000589628.1:n.106C>G
(RTN2)
|
|
|
ENST00000590526.5:c.317C>G
(RTN2)
|
ENSP00000466619.1:p.Ala106Gly
|
|
ENST00000590746.5:n.62-3335C>G
(RTN2)
|
|
|
ENST00000591286.5:c.*137C>G
(RTN2)
|
ENSP00000467863.1:n.*137C>G
|
|
NM_005619.4:c.1139C>G
(RTN2)
|
NP_005610.1:p.Ala380Gly
|
|
NM_206900.2:c.920C>G
(RTN2)
|
NP_996783.1:p.Ala307Gly
|
|
NM_206901.2:c.119C>G
(RTN2)
|
NP_996784.1:p.Ala40Gly
|
|
NM_005619.5:c.1139C>G
(RTN2)
MANE Select
|
NP_005610.1:p.Ala380Gly
|
|
NM_206900.3:c.920C>G
(RTN2)
|
NP_996783.1:p.Ala307Gly
|
|
NM_206901.3:c.119C>G
(RTN2)
|
NP_996784.1:p.Ala40Gly
|
|