ENST00000636937.2:c.1544T>C
|
ENSP00000516154.1:p.Ile515Thr
|
|
ENST00000268124.11:c.1544T>C
MANE Select
|
ENSP00000268124.5:p.Ile515Thr
|
|
ENST00000530292.3:c.1145T>C
|
ENSP00000432885.2:p.Ile382Thr
|
|
ENST00000635986.2:c.1544T>C
|
ENSP00000490653.2:p.Ile515Thr
|
|
ENST00000636774.1:c.*111T>C
|
ENSP00000489799.1:n.*111T>C
|
|
ENST00000637238.1:c.281T>C
|
ENSP00000490756.1:p.Ile94Thr
|
|
ENST00000637264.1:c.616T>C
|
|
|
ENST00000666746.1:c.1121T>C
|
|
|
ENST00000672071.1:n.1742T>C
|
|
|
ENST00000672923.2:n.1647T>C
|
|
|
ENST00000268124.9:c.1544T>C
|
ENSP00000268124.5:p.Ile515Thr
|
|
ENST00000442287.6:c.1544T>C
|
ENSP00000399851.2:p.Ile515Thr
|
|
ENST00000631044.2:c.*927T>C
|
ENSP00000486730.1:n.*927T>C
|
|
NM_001126131.1:c.1544T>C
|
NP_001119603.1:p.Ile515Thr
|
|
NM_002693.2:c.1544T>C
|
NP_002684.1:p.Ile515Thr
|
|
NM_001126131.2:c.1544T>C
|
NP_001119603.1:p.Ile515Thr
|
|
NM_002693.3:c.1544T>C
MANE Select
|
NP_002684.1:p.Ile515Thr
|
|