ENST00000400521.7:c.298G>A
MANE Select
|
ENSP00000383365.1:p.Ala100Thr
|
|
ENST00000334363.14:c.298G>A
|
ENSP00000334451.9:p.Ala100Thr
|
|
ENST00000400518.5:c.208G>A
|
ENSP00000383362.1:p.Ala70Thr
|
|
ENST00000400519.6:c.295G>A
|
ENSP00000383363.1:p.Ala99Thr
|
|
ENST00000400521.6:c.298G>A
|
ENSP00000383365.1:p.Ala100Thr
|
|
ENST00000400525.6:c.229G>A
|
ENSP00000383369.3:p.Ala77Thr
|
|
ENST00000474308.5:c.241G>A
|
ENSP00000485665.1:p.Ala81Thr
|
|
ENST00000491939.6:c.202G>A
|
ENSP00000485543.1:p.Ala68Thr
|
|
ENST00000496729.2:n.303G>A
|
|
|
ENST00000542719.6:c.10G>A
|
ENSP00000485128.2:p.Ala4Thr
|
|
NM_001282512.1:c.298G>A
|
NP_001269441.1:p.Ala100Thr
|
|
NM_006440.4:c.298G>A
|
NP_006431.2:p.Ala100Thr
|
|
NM_001282512.2:c.298G>A
|
NP_001269441.1:p.Ala100Thr
|
|
NM_001352300.1:c.295G>A
|
NP_001339229.1:p.Ala99Thr
|
|
NM_001352301.1:c.208G>A
|
NP_001339230.1:p.Ala70Thr
|
|
NM_001352302.1:c.10G>A
|
NP_001339231.1:p.Ala4Thr
|
|
NM_001352303.1:c.202G>A
|
NP_001339232.1:p.Ala68Thr
|
|
NR_147957.1:n.430G>A
|
|
|
NM_006440.5:c.298G>A
MANE Select
|
NP_006431.2:p.Ala100Thr
|
|
NM_001282512.3:c.298G>A
|
NP_001269441.1:p.Ala100Thr
|
|
NM_001352300.2:c.295G>A
|
NP_001339229.1:p.Ala99Thr
|
|
NR_147957.2:n.256G>A
|
|
|
NM_001352301.2:c.208G>A
|
NP_001339230.1:p.Ala70Thr
|
|
NM_001352302.2:c.10G>A
|
NP_001339231.1:p.Ala4Thr
|
|
NM_001352303.2:c.202G>A
|
NP_001339232.1:p.Ala68Thr
|
|