ENST00000245923.9:c.1086A>C
(RTN2)
MANE Select
|
ENSP00000245923.3:p.Thr362=
|
|
ENST00000245923.8:c.1086A>C
(RTN2)
|
ENSP00000245923.3:p.Thr362=
|
|
ENST00000344680.8:c.867A>C
(RTN2)
|
ENSP00000345127.3:p.Thr289=
|
|
ENST00000401705.5:c.-16+522T>G
(PPM1N)
|
ENSP00000384318.1:n.-16+522T>G
|
|
ENST00000430715.6:c.66A>C
(RTN2)
|
ENSP00000398178.1:p.Thr22=
|
|
ENST00000587597.5:c.1086A>C
(RTN2)
|
ENSP00000468144.1:p.Thr362=
|
|
ENST00000588036.5:n.80-515A>C
(RTN2)
|
|
|
ENST00000589628.1:n.53A>C
(RTN2)
|
|
|
ENST00000590526.5:c.264A>C
(RTN2)
|
ENSP00000466619.1:p.Thr88=
|
|
ENST00000590746.5:n.62-3388A>C
(RTN2)
|
|
|
ENST00000591286.5:c.*84A>C
(RTN2)
|
ENSP00000467863.1:n.*84A>C
|
|
NM_005619.4:c.1086A>C
(RTN2)
|
NP_005610.1:p.Thr362=
|
|
NM_206900.2:c.867A>C
(RTN2)
|
NP_996783.1:p.Thr289=
|
|
NM_206901.2:c.66A>C
(RTN2)
|
NP_996784.1:p.Thr22=
|
|
NM_005619.5:c.1086A>C
(RTN2)
MANE Select
|
NP_005610.1:p.Thr362=
|
|
NM_206900.3:c.867A>C
(RTN2)
|
NP_996783.1:p.Thr289=
|
|
NM_206901.3:c.66A>C
(RTN2)
|
NP_996784.1:p.Thr22=
|
|