ENST00000682114.1:c.441C>G
|
ENSP00000507245.1:p.Cys147Trp
|
|
ENST00000682478.1:n.631C>G
|
|
|
ENST00000683576.1:n.631C>G
|
|
|
ENST00000683627.1:c.441C>G
|
ENSP00000507533.1:p.Cys147Trp
|
|
ENST00000684082.1:c.398C>G
|
ENSP00000508266.1:n.398C>G
|
|
ENST00000684633.1:n.413C>G
|
|
|
ENST00000684678.1:c.437C>G
|
ENSP00000507059.1:n.437C>G
|
|
ENST00000369842.9:c.441C>G
MANE Select
|
ENSP00000358857.4:p.Cys147Trp
|
|
ENST00000369835.3:c.336C>G
|
ENSP00000358850.3:p.Cys112Trp
|
|
ENST00000369842.8:c.441C>G
|
ENSP00000358857.4:p.Cys147Trp
|
|
ENST00000428228.5:c.*346C>G
|
ENSP00000401081.1:n.*346C>G
|
|
ENST00000468294.5:n.401C>G
|
|
|
ENST00000471965.1:n.230C>G
|
|
|
ENST00000485261.1:n.631C>G
|
|
|
ENST00000486738.5:n.799C>G
|
|
|
ENST00000492448.1:n.424C>G
|
|
|
NM_000117.2:c.441C>G , LRG_745t1:c.441C>G
|
NP_000108.1:p.Cys147Trp
|
|
XM_024452349.1:c.447C>G
|
XP_024308117.1:p.Cys149Trp
|
|
NM_000117.3:c.441C>G
MANE Select
|
NP_000108.1:p.Cys147Trp
|
|