ENST00000682114.1:c.450G>T
|
ENSP00000507245.1:p.Arg150Ser
|
|
ENST00000682478.1:n.640G>T
|
|
|
ENST00000683576.1:n.640G>T
|
|
|
ENST00000683627.1:c.450G>T
|
ENSP00000507533.1:p.Arg150Ser
|
|
ENST00000684082.1:c.407G>T
|
ENSP00000508266.1:n.407G>T
|
|
ENST00000684633.1:n.422G>T
|
|
|
ENST00000684678.1:c.446G>T
|
ENSP00000507059.1:n.446G>T
|
|
ENST00000369842.9:c.450G>T
MANE Select
|
ENSP00000358857.4:p.Arg150Ser
|
|
ENST00000369835.3:c.345G>T
|
ENSP00000358850.3:p.Arg115Ser
|
|
ENST00000369842.8:c.450G>T
|
ENSP00000358857.4:p.Arg150Ser
|
|
ENST00000428228.5:c.*355G>T
|
ENSP00000401081.1:n.*355G>T
|
|
ENST00000468294.5:n.489G>T
|
|
|
ENST00000471965.1:n.239G>T
|
|
|
ENST00000485261.1:n.719G>T
|
|
|
ENST00000486738.5:n.887G>T
|
|
|
ENST00000492448.1:n.433G>T
|
|
|
NM_000117.2:c.450G>T , LRG_745t1:c.450G>T
|
NP_000108.1:p.Arg150Ser
|
|
XM_024452349.1:c.456G>T
|
XP_024308117.1:p.Arg152Ser
|
|
NM_000117.3:c.450G>T
MANE Select
|
NP_000108.1:p.Arg150Ser
|
|