ENST00000333213.11:c.717A>C
MANE Select
|
ENSP00000327487.6:p.Gln239His
|
|
ENST00000434205.8:c.414A>C
|
ENSP00000406559.4:p.Gln138His
|
|
ENST00000545228.3:c.717A>C
|
ENSP00000438169.3:p.Gln239His
|
|
ENST00000579449.2:n.516A>C
|
|
|
ENST00000580013.6:n.920A>C
|
|
|
ENST00000583818.2:c.771A>C
|
ENSP00000461928.2:n.771A>C
|
|
ENST00000679370.1:n.1298A>C
|
|
|
ENST00000679429.1:c.*175A>C
|
ENSP00000505403.1:n.*175A>C
|
|
ENST00000679443.1:n.786A>C
|
|
|
ENST00000679782.1:c.717A>C
|
ENSP00000505995.1:p.Gln239His
|
|
ENST00000679919.1:n.786A>C
|
|
|
ENST00000679928.1:c.*328A>C
|
ENSP00000506071.1:n.*328A>C
|
|
ENST00000680528.1:n.742A>C
|
|
|
ENST00000680999.1:c.717A>C
|
ENSP00000504984.1:p.Gln239His
|
|
ENST00000681282.1:c.746A>C
|
ENSP00000506339.1:p.Asn249Thr
|
|
ENST00000333213.10:c.717A>C
|
ENSP00000327487.6:p.Gln239His
|
|
ENST00000578415.1:c.677A>C
|
|
|
ENST00000583173.5:c.459-209A>C
|
ENSP00000463619.1:n.459-209A>C
|
|
ENST00000583818.1:c.666A>C
|
ENSP00000461928.1:n.666A>C
|
|
NM_207346.2:c.717A>C
|
NP_997229.2:p.Gln239His
|
|
XM_005257229.2:c.717A>C
|
XP_005257286.1:p.Gln239His
|
|
XM_006721821.2:c.414A>C
|
XP_006721884.1:p.Gln138His
|
|
XM_011524616.1:c.717A>C
|
XP_011522918.1:p.Gln239His
|
|
XM_011524617.1:c.717A>C
|
XP_011522919.1:p.Gln239His
|
|
XM_011524618.1:c.717A>C
|
XP_011522920.1:p.Gln239His
|
|
XR_243646.2:n.747A>C
|
|
|
XM_005257229.4:c.717A>C
|
XP_005257286.1:p.Gln239His
|
|
XR_243646.4:n.753A>C
|
|
|
NM_207346.3:c.717A>C
MANE Select
|
NP_997229.2:p.Gln239His
|
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