ENST00000682114.1:c.115T>G
|
ENSP00000507245.1:p.Phe39Val
|
|
ENST00000682478.1:n.91T>G
|
|
|
ENST00000683576.1:n.91T>G
|
|
|
ENST00000683627.1:c.115T>G
|
ENSP00000507533.1:p.Phe39Val
|
|
ENST00000684082.1:c.115T>G
|
ENSP00000508266.1:p.Phe39Val
|
|
ENST00000684633.1:n.87T>G
|
|
|
ENST00000684678.1:c.111T>G
|
ENSP00000507059.1:p.Ser37=
|
|
ENST00000369842.9:c.115T>G
MANE Select
|
ENSP00000358857.4:p.Phe39Val
|
|
ENST00000369835.3:c.82+156T>G
|
ENSP00000358850.3:n.82+156T>G
|
|
ENST00000369842.8:c.115T>G
|
ENSP00000358857.4:p.Phe39Val
|
|
ENST00000428228.5:c.*20T>G
|
ENSP00000401081.1:n.*20T>G
|
|
ENST00000468294.5:n.75T>G
|
|
|
ENST00000485261.1:n.163+156T>G
|
|
|
ENST00000486738.5:n.259T>G
|
|
|
ENST00000492448.1:n.98T>G
|
|
|
ENST00000494443.5:n.172T>G
|
|
|
NM_000117.2:c.115T>G , LRG_745t1:c.115T>G
|
NP_000108.1:p.Phe39Val
|
|
XM_024452349.1:c.-94T>G
|
XP_024308117.1:n.-94T>G
|
|
NM_000117.3:c.115T>G
MANE Select
|
NP_000108.1:p.Phe39Val
|
|