ENST00000682114.1:c.258G>T
|
ENSP00000507245.1:p.Gln86His
|
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ENST00000682478.1:n.234G>T
|
|
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ENST00000683576.1:n.234G>T
|
|
|
ENST00000683627.1:c.258G>T
|
ENSP00000507533.1:p.Gln86His
|
|
ENST00000684082.1:c.258G>T
|
ENSP00000508266.1:p.Gln86His
|
|
ENST00000684633.1:n.230G>T
|
|
|
ENST00000684678.1:c.254G>T
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ENSP00000507059.1:n.254G>T
|
|
ENST00000369842.9:c.258G>T
MANE Select
|
ENSP00000358857.4:p.Gln86His
|
|
ENST00000369835.3:c.153G>T
|
ENSP00000358850.3:p.Gln51His
|
|
ENST00000369842.8:c.258G>T
|
ENSP00000358857.4:p.Gln86His
|
|
ENST00000428228.5:c.*163G>T
|
ENSP00000401081.1:n.*163G>T
|
|
ENST00000468294.5:n.218G>T
|
|
|
ENST00000485261.1:n.234G>T
|
|
|
ENST00000486738.5:n.402G>T
|
|
|
ENST00000492448.1:n.241G>T
|
|
|
ENST00000494443.5:n.315G>T
|
|
|
NM_000117.2:c.258G>T , LRG_745t1:c.258G>T
|
NP_000108.1:p.Gln86His
|
|
XM_024452349.1:c.50G>T
|
XP_024308117.1:p.Arg17Ile
|
|
NM_000117.3:c.258G>T
MANE Select
|
NP_000108.1:p.Gln86His
|
|