ENST00000650793.2:n.291T>C
|
|
|
ENST00000697612.1:n.969T>C
|
|
|
ENST00000374881.3:c.258T>C
|
ENSP00000364015.2:p.Ser86=
|
|
ENST00000374882.8:c.270T>C
MANE Select
|
ENSP00000364016.4:p.Ser90=
|
|
ENST00000650411.1:n.1591T>C
|
|
|
ENST00000650793.1:n.291T>C
|
|
|
ENST00000374881.2:c.258T>C
|
ENSP00000364015.2:p.Ser86=
|
|
ENST00000374882.7:c.270T>C
|
ENSP00000364016.3:p.Ser90=
|
|
ENST00000395339.7:c.270T>C
|
ENSP00000378748.3:p.Ser90=
|
|
ENST00000484003.1:n.496T>C
|
|
|
NM_004159.4:c.258T>C
|
NP_004150.1:p.Ser86=
|
|
NM_148919.3:c.270T>C
|
NP_683720.2:p.Ser90=
|
|
NM_148919.4:c.270T>C
MANE Select
|
NP_683720.2:p.Ser90=
|
|
NM_004159.5:c.258T>C
|
NP_004150.1:p.Ser86=
|
|