ENST00000400521.7:c.807A>T
MANE Select
|
ENSP00000383365.1:p.Ala269=
|
|
ENST00000334363.14:c.807A>T
|
ENSP00000334451.9:p.Ala269=
|
|
ENST00000400518.5:c.717A>T
|
ENSP00000383362.1:p.Ala239=
|
|
ENST00000400519.6:c.804A>T
|
ENSP00000383363.1:p.Ala268=
|
|
ENST00000400521.6:c.807A>T
|
ENSP00000383365.1:p.Ala269=
|
|
ENST00000400525.6:c.738A>T
|
ENSP00000383369.3:p.Ala246=
|
|
ENST00000474308.5:c.750A>T
|
ENSP00000485665.1:p.Ala250=
|
|
ENST00000475995.3:c.304A>T
|
|
|
ENST00000491939.6:c.711A>T
|
ENSP00000485543.1:p.Ala237=
|
|
ENST00000494454.5:n.881A>T
|
|
|
ENST00000542719.6:c.519A>T
|
ENSP00000485128.2:p.Ala173=
|
|
ENST00000634537.1:c.36A>T
|
ENSP00000489208.1:p.Ala12=
|
|
ENST00000635155.1:n.393A>T
|
|
|
NM_001282512.1:c.807A>T
|
NP_001269441.1:p.Ala269=
|
|
NM_006440.4:c.807A>T
|
NP_006431.2:p.Ala269=
|
|
NM_001282512.2:c.807A>T
|
NP_001269441.1:p.Ala269=
|
|
NM_001352300.1:c.804A>T
|
NP_001339229.1:p.Ala268=
|
|
NM_001352301.1:c.717A>T
|
NP_001339230.1:p.Ala239=
|
|
NM_001352302.1:c.519A>T
|
NP_001339231.1:p.Ala173=
|
|
NM_001352303.1:c.711A>T
|
NP_001339232.1:p.Ala237=
|
|
NR_147957.1:n.939A>T
|
|
|
NM_006440.5:c.807A>T
MANE Select
|
NP_006431.2:p.Ala269=
|
|
NM_001282512.3:c.807A>T
|
NP_001269441.1:p.Ala269=
|
|
NM_001352300.2:c.804A>T
|
NP_001339229.1:p.Ala268=
|
|
NR_147957.2:n.765A>T
|
|
|
NM_001352301.2:c.717A>T
|
NP_001339230.1:p.Ala239=
|
|
NM_001352302.2:c.519A>T
|
NP_001339231.1:p.Ala173=
|
|
NM_001352303.2:c.711A>T
|
NP_001339232.1:p.Ala237=
|
|