ENST00000650793.2:n.586G>T
|
|
|
ENST00000697612.1:n.1264G>T
|
|
|
ENST00000374881.3:c.395G>T
|
ENSP00000364015.2:p.Arg132Met
|
|
ENST00000374882.8:c.407G>T
MANE Select
|
ENSP00000364016.4:p.Arg136Met
|
|
ENST00000650411.1:n.1728G>T
|
|
|
ENST00000650793.1:n.586G>T
|
|
|
ENST00000374881.2:c.395G>T
|
ENSP00000364015.2:p.Arg132Met
|
|
ENST00000374882.7:c.407G>T
|
ENSP00000364016.3:p.Arg136Met
|
|
ENST00000395339.7:c.335G>T
|
ENSP00000378748.3:p.Arg112Met
|
|
ENST00000484003.1:n.791G>T
|
|
|
NM_004159.4:c.395G>T
|
NP_004150.1:p.Arg132Met
|
|
NM_148919.3:c.407G>T
|
NP_683720.2:p.Arg136Met
|
|
NM_148919.4:c.407G>T
MANE Select
|
NP_683720.2:p.Arg136Met
|
|
NM_004159.5:c.395G>T
|
NP_004150.1:p.Arg132Met
|
|