ENST00000379727.8:c.1393T>C
MANE Select
|
ENSP00000369050.3:p.Trp465Arg
|
|
ENST00000379727.7:c.1393T>C
|
ENSP00000369050.3:p.Trp465Arg
|
|
ENST00000395048.6:c.1393T>C
|
ENSP00000378488.2:p.Trp465Arg
|
|
ENST00000395049.8:c.1306T>C
|
ENSP00000378489.4:p.Trp436Arg
|
|
ENST00000567032.5:c.1393T>C
|
ENSP00000456585.1:p.Trp465Arg
|
|
ENST00000612821.4:c.1309T>C
|
ENSP00000479744.1:p.Trp437Arg
|
|
ENST00000617691.4:c.1306T>C
|
ENSP00000482863.1:p.Trp436Arg
|
|
NM_000499.3:c.1393T>C
|
NP_000490.1:p.Trp465Arg
|
|
XM_005254185.1:c.1393T>C
|
XP_005254242.1:p.Trp465Arg
|
|
NM_000499.5:c.1393T>C
|
NP_000490.1:p.Trp465Arg
|
|
NM_001319216.2:c.1306T>C
|
NP_001306145.1:p.Trp436Arg
|
|
NM_001319217.2:c.1393T>C
MANE Select
|
NP_001306146.1:p.Trp465Arg
|
|