ENST00000636937.2:c.1484T>C
|
ENSP00000516154.1:p.Phe495Ser
|
|
ENST00000268124.11:c.1484T>C
MANE Select
|
ENSP00000268124.5:p.Phe495Ser
|
|
ENST00000530292.3:c.1085T>C
|
ENSP00000432885.2:p.Phe362Ser
|
|
ENST00000635986.2:c.1484T>C
|
ENSP00000490653.2:p.Phe495Ser
|
|
ENST00000636774.1:c.*51T>C
|
ENSP00000489799.1:n.*51T>C
|
|
ENST00000637238.1:c.221T>C
|
ENSP00000490756.1:p.Phe74Ser
|
|
ENST00000637264.1:c.556T>C
|
|
|
ENST00000666746.1:c.1061T>C
|
|
|
ENST00000672071.1:n.1682T>C
|
|
|
ENST00000672923.2:n.1587T>C
|
|
|
ENST00000268124.9:c.1484T>C
|
ENSP00000268124.5:p.Phe495Ser
|
|
ENST00000442287.6:c.1484T>C
|
ENSP00000399851.2:p.Phe495Ser
|
|
ENST00000532363.2:n.445T>C
|
|
|
ENST00000631044.2:c.*867T>C
|
ENSP00000486730.1:n.*867T>C
|
|
NM_001126131.1:c.1484T>C
|
NP_001119603.1:p.Phe495Ser
|
|
NM_002693.2:c.1484T>C
|
NP_002684.1:p.Phe495Ser
|
|
NM_001126131.2:c.1484T>C
|
NP_001119603.1:p.Phe495Ser
|
|
NM_002693.3:c.1484T>C
MANE Select
|
NP_002684.1:p.Phe495Ser
|
|