ENST00000682114.1:c.90T>G
|
ENSP00000507245.1:p.Thr30=
|
|
ENST00000682478.1:n.66T>G
|
|
|
ENST00000683576.1:n.66T>G
|
|
|
ENST00000683627.1:c.90T>G
|
ENSP00000507533.1:p.Thr30=
|
|
ENST00000684082.1:c.90T>G
|
ENSP00000508266.1:p.Thr30=
|
|
ENST00000684633.1:n.62T>G
|
|
|
ENST00000684678.1:c.86T>G
|
ENSP00000507059.1:p.Leu29Arg
|
|
ENST00000369842.9:c.90T>G
MANE Select
|
ENSP00000358857.4:p.Thr30=
|
|
ENST00000369835.3:c.82+131T>G
|
ENSP00000358850.3:n.82+131T>G
|
|
ENST00000369842.8:c.90T>G
|
ENSP00000358857.4:p.Thr30=
|
|
ENST00000428228.5:c.61T>G
|
ENSP00000401081.1:p.Ser21Ala
|
|
ENST00000468294.5:n.50T>G
|
|
|
ENST00000485261.1:n.163+131T>G
|
|
|
ENST00000486738.5:n.234T>G
|
|
|
ENST00000492448.1:n.73T>G
|
|
|
ENST00000494443.5:n.147T>G
|
|
|
NM_000117.2:c.90T>G , LRG_745t1:c.90T>G
|
NP_000108.1:p.Thr30=
|
|
XM_024452349.1:c.-119T>G
|
XP_024308117.1:n.-119T>G
|
|
NM_000117.3:c.90T>G
MANE Select
|
NP_000108.1:p.Thr30=
|
|