ENST00000330540.7:c.948T>C
MANE Select
|
ENSP00000332049.2:p.Ser316=
|
|
ENST00000264468.9:c.786T>C
|
ENSP00000264468.6:p.Ser262=
|
|
ENST00000330540.6:c.948T>C
|
ENSP00000332049.2:p.Ser316=
|
|
ENST00000393627.6:c.930T>C
|
ENSP00000377248.2:p.Ser310=
|
|
ENST00000469710.5:c.702T>C
|
ENSP00000418988.1:p.Ser234=
|
|
ENST00000478741.1:c.790T>C
|
|
|
ENST00000493101.5:c.612T>C
|
ENSP00000420230.1:p.Ser204=
|
|
NM_001206924.1:c.612T>C
|
NP_001193853.1:p.Ser204=
|
|
NM_001206925.1:c.702T>C
|
NP_001193854.1:p.Ser234=
|
|
NM_006889.4:c.930T>C
|
NP_008820.3:p.Ser310=
|
|
NM_175862.4:c.948T>C
|
NP_787058.4:p.Ser316=
|
|
NM_176892.1:c.786T>C
|
NP_795711.1:p.Ser262=
|
|
NM_175862.5:c.948T>C
MANE Select
|
NP_787058.5:p.Ser316=
|
|
NM_001206924.2:c.612T>C
|
NP_001193853.2:p.Ser204=
|
|
NM_001206925.2:c.702T>C
|
NP_001193854.2:p.Ser234=
|
|
NM_006889.5:c.930T>C
|
NP_008820.4:p.Ser310=
|
|
NM_176892.2:c.786T>C
|
NP_795711.2:p.Ser262=
|
|