ENST00000650793.2:n.287A>T
|
|
|
ENST00000697612.1:n.965A>T
|
|
|
ENST00000374881.3:c.254A>T
|
ENSP00000364015.2:p.Asp85Val
|
|
ENST00000374882.8:c.266A>T
MANE Select
|
ENSP00000364016.4:p.Asp89Val
|
|
ENST00000650411.1:n.1587A>T
|
|
|
ENST00000650793.1:n.287A>T
|
|
|
ENST00000374881.2:c.254A>T
|
ENSP00000364015.2:p.Asp85Val
|
|
ENST00000374882.7:c.266A>T
|
ENSP00000364016.3:p.Asp89Val
|
|
ENST00000395339.7:c.266A>T
|
ENSP00000378748.3:p.Asp89Val
|
|
ENST00000484003.1:n.492A>T
|
|
|
NM_004159.4:c.254A>T
|
NP_004150.1:p.Asp85Val
|
|
NM_148919.3:c.266A>T
|
NP_683720.2:p.Asp89Val
|
|
NM_148919.4:c.266A>T
MANE Select
|
NP_683720.2:p.Asp89Val
|
|
NM_004159.5:c.254A>T
|
NP_004150.1:p.Asp85Val
|
|