ENST00000636937.2:c.3427G>T
|
ENSP00000516154.1:p.Glu1143Ter
|
|
ENST00000268124.11:c.3427G>T
MANE Select
|
ENSP00000268124.5:p.Glu1143Ter
|
|
ENST00000530292.3:c.3028G>T
|
ENSP00000432885.2:p.Glu1010Ter
|
|
ENST00000635986.2:c.*497G>T
|
ENSP00000490653.2:n.*497G>T
|
|
ENST00000636774.1:c.*1994G>T
|
ENSP00000489799.1:n.*1994G>T
|
|
ENST00000637238.1:c.2236G>T
|
ENSP00000490756.1:n.2236G>T
|
|
ENST00000637264.1:c.2499G>T
|
|
|
ENST00000666746.1:c.3004G>T
|
|
|
ENST00000672071.1:n.3625G>T
|
|
|
ENST00000672695.1:n.604G>T
|
|
|
ENST00000672923.2:n.3427G>T
|
|
|
ENST00000268124.9:c.3427G>T
|
ENSP00000268124.5:p.Glu1143Ter
|
|
ENST00000442287.6:c.3427G>T
|
ENSP00000399851.2:p.Glu1143Ter
|
|
ENST00000530292.2:c.511G>T
|
ENSP00000432885.1:p.Glu171Ter
|
|
ENST00000631044.2:c.*2851G>T
|
ENSP00000486730.1:n.*2851G>T
|
|
NM_001126131.1:c.3427G>T
|
NP_001119603.1:p.Glu1143Ter
|
|
NM_002693.2:c.3427G>T
|
NP_002684.1:p.Glu1143Ter
|
|
NM_001126131.2:c.3427G>T
|
NP_001119603.1:p.Glu1143Ter
|
|
NM_002693.3:c.3427G>T
MANE Select
|
NP_002684.1:p.Glu1143Ter
|
|