ENST00000636937.2:c.3402T>C
|
ENSP00000516154.1:p.His1134=
|
|
ENST00000268124.11:c.3402T>C
MANE Select
|
ENSP00000268124.5:p.His1134=
|
|
ENST00000530292.3:c.3003T>C
|
ENSP00000432885.2:p.His1001=
|
|
ENST00000635986.2:c.*472T>C
|
ENSP00000490653.2:n.*472T>C
|
|
ENST00000636774.1:c.*1969T>C
|
ENSP00000489799.1:n.*1969T>C
|
|
ENST00000637238.1:c.2211T>C
|
ENSP00000490756.1:n.2211T>C
|
|
ENST00000637264.1:c.2474T>C
|
|
|
ENST00000666746.1:c.2979T>C
|
|
|
ENST00000672071.1:n.3600T>C
|
|
|
ENST00000672695.1:n.579T>C
|
|
|
ENST00000672923.2:n.3402T>C
|
|
|
ENST00000268124.9:c.3402T>C
|
ENSP00000268124.5:p.His1134=
|
|
ENST00000442287.6:c.3402T>C
|
ENSP00000399851.2:p.His1134=
|
|
ENST00000530292.2:c.486T>C
|
ENSP00000432885.1:p.His162=
|
|
ENST00000631044.2:c.*2826T>C
|
ENSP00000486730.1:n.*2826T>C
|
|
NM_001126131.1:c.3402T>C
|
NP_001119603.1:p.His1134=
|
|
NM_002693.2:c.3402T>C
|
NP_002684.1:p.His1134=
|
|
NM_001126131.2:c.3402T>C
|
NP_001119603.1:p.His1134=
|
|
NM_002693.3:c.3402T>C
MANE Select
|
NP_002684.1:p.His1134=
|
|