ENST00000636937.2:c.3590G>T
|
ENSP00000516154.1:p.Cys1197Phe
|
|
ENST00000268124.11:c.3590G>T
MANE Select
|
ENSP00000268124.5:p.Cys1197Phe
|
|
ENST00000530292.3:c.3290G>T
|
ENSP00000432885.2:n.3290G>T
|
|
ENST00000635986.2:c.*660G>T
|
ENSP00000490653.2:n.*660G>T
|
|
ENST00000636774.1:c.*2194G>T
|
ENSP00000489799.1:n.*2194G>T
|
|
ENST00000637238.1:c.2498G>T
|
ENSP00000490756.1:n.2498G>T
|
|
ENST00000637264.1:c.2602G>T
|
|
|
ENST00000666746.1:c.3167G>T
|
|
|
ENST00000672071.1:n.4792G>T
|
|
|
ENST00000672695.1:n.1369G>T
|
|
|
ENST00000672923.2:n.3590G>T
|
|
|
ENST00000268124.9:c.3590G>T
|
ENSP00000268124.5:p.Cys1197Phe
|
|
ENST00000442287.6:c.3590G>T
|
ENSP00000399851.2:p.Cys1197Phe
|
|
ENST00000526671.1:n.400G>T
|
|
|
ENST00000530292.2:c.773G>T
|
ENSP00000432885.1:n.773G>T
|
|
ENST00000631044.2:c.*3014G>T
|
ENSP00000486730.1:n.*3014G>T
|
|
NM_001126131.1:c.3590G>T
|
NP_001119603.1:p.Cys1197Phe
|
|
NM_002693.2:c.3590G>T
|
NP_002684.1:p.Cys1197Phe
|
|
NM_001126131.2:c.3590G>T
|
NP_001119603.1:p.Cys1197Phe
|
|
NM_002693.3:c.3590G>T
MANE Select
|
NP_002684.1:p.Cys1197Phe
|
|