ENST00000246337.9:c.995G=
MANE Select
|
ENSP00000246337.4:p.Arg332=
|
|
ENST00000491773.6:c.752G=
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ENSP00000498551.1:p.Arg251=
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ENST00000636293.1:c.857G=
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ENSP00000490710.1:p.Arg286=
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ENST00000636836.1:c.*31G=
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ENSP00000490594.1:n.*31G=
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ENST00000651476.1:c.890G=
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ENSP00000498668.1:p.Arg297=
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ENST00000652165.1:c.752G=
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ENSP00000498295.1:p.Arg251=
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|
ENST00000652287.1:c.932G=
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ENSP00000498413.1:p.Arg311=
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|
ENST00000652514.1:c.956G=
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ENSP00000498635.1:n.956G=
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|
ENST00000246337.8:c.995G=
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ENSP00000246337.4:p.Arg332=
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|
ENST00000465678.1:n.740G=
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|
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ENST00000466193.1:n.521G=
|
|
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ENST00000472254.1:n.748G=
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|
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ENST00000494399.5:n.1662G=
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|
|
NM_000374.4:c.995G=
|
NP_000365.3:p.Arg332=
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|
NR_036510.1:n.1178G=
|
|
|
XM_005271169.1:c.779G=
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XP_005271226.1:p.Arg260=
|
|
XM_005271170.1:c.779G=
|
XP_005271227.1:p.Arg260=
|
|
XM_011542080.1:c.932G=
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XP_011540382.1:p.Arg311=
|
|
XM_011542081.1:c.827G=
|
XP_011540383.1:p.Arg276=
|
|
NM_000374.5:c.995G=
MANE Select
|
NP_000365.3:p.Arg332=
|
|
NR_158184.1:n.1076G=
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|
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NR_158185.1:n.1026G=
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NR_036510.2:n.1057G=
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