ENST00000400521.7:c.327T>C
MANE Select
|
ENSP00000383365.1:p.Asp109=
|
|
ENST00000334363.14:c.327T>C
|
ENSP00000334451.9:p.Asp109=
|
|
ENST00000400518.5:c.237T>C
|
ENSP00000383362.1:p.Asp79=
|
|
ENST00000400519.6:c.324T>C
|
ENSP00000383363.1:p.Asp108=
|
|
ENST00000400521.6:c.327T>C
|
ENSP00000383365.1:p.Asp109=
|
|
ENST00000400525.6:c.258T>C
|
ENSP00000383369.3:p.Asp86=
|
|
ENST00000474308.5:c.270T>C
|
ENSP00000485665.1:p.Asp90=
|
|
ENST00000491939.6:c.231T>C
|
ENSP00000485543.1:p.Asp77=
|
|
ENST00000496729.2:n.332T>C
|
|
|
ENST00000542719.6:c.39T>C
|
ENSP00000485128.2:p.Asp13=
|
|
NM_001282512.1:c.327T>C
|
NP_001269441.1:p.Asp109=
|
|
NM_006440.4:c.327T>C
|
NP_006431.2:p.Asp109=
|
|
NM_001282512.2:c.327T>C
|
NP_001269441.1:p.Asp109=
|
|
NM_001352300.1:c.324T>C
|
NP_001339229.1:p.Asp108=
|
|
NM_001352301.1:c.237T>C
|
NP_001339230.1:p.Asp79=
|
|
NM_001352302.1:c.39T>C
|
NP_001339231.1:p.Asp13=
|
|
NM_001352303.1:c.231T>C
|
NP_001339232.1:p.Asp77=
|
|
NR_147957.1:n.459T>C
|
|
|
NM_006440.5:c.327T>C
MANE Select
|
NP_006431.2:p.Asp109=
|
|
NM_001282512.3:c.327T>C
|
NP_001269441.1:p.Asp109=
|
|
NM_001352300.2:c.324T>C
|
NP_001339229.1:p.Asp108=
|
|
NR_147957.2:n.285T>C
|
|
|
NM_001352301.2:c.237T>C
|
NP_001339230.1:p.Asp79=
|
|
NM_001352302.2:c.39T>C
|
NP_001339231.1:p.Asp13=
|
|
NM_001352303.2:c.231T>C
|
NP_001339232.1:p.Asp77=
|
|