ENST00000636937.2:c.938T>C
|
ENSP00000516154.1:p.Ile313Thr
|
|
ENST00000268124.11:c.938T>C
MANE Select
|
ENSP00000268124.5:p.Ile313Thr
|
|
ENST00000530292.3:c.539T>C
|
ENSP00000432885.2:p.Ile180Thr
|
|
ENST00000635986.2:c.938T>C
|
ENSP00000490653.2:p.Ile313Thr
|
|
ENST00000636774.1:c.938T>C
|
ENSP00000489799.1:p.Ile313Thr
|
|
ENST00000637264.1:c.10T>C
|
|
|
ENST00000666746.1:c.595T>C
|
|
|
ENST00000672071.1:n.1136T>C
|
|
|
ENST00000268124.9:c.938T>C
|
ENSP00000268124.5:p.Ile313Thr
|
|
ENST00000442287.6:c.938T>C
|
ENSP00000399851.2:p.Ile313Thr
|
|
ENST00000631044.2:c.*321T>C
|
ENSP00000486730.1:n.*321T>C
|
|
NM_001126131.1:c.938T>C
|
NP_001119603.1:p.Ile313Thr
|
|
NM_002693.2:c.938T>C
|
NP_002684.1:p.Ile313Thr
|
|
NM_001126131.2:c.938T>C
|
NP_001119603.1:p.Ile313Thr
|
|
NM_002693.3:c.938T>C
MANE Select
|
NP_002684.1:p.Ile313Thr
|
|