ENST00000400521.7:c.928G>T
MANE Select
|
ENSP00000383365.1:p.Asp310Tyr
|
|
ENST00000334363.14:c.928G>T
|
ENSP00000334451.9:p.Asp310Tyr
|
|
ENST00000400518.5:c.838G>T
|
ENSP00000383362.1:p.Asp280Tyr
|
|
ENST00000400519.6:c.925G>T
|
ENSP00000383363.1:p.Asp309Tyr
|
|
ENST00000400521.6:c.928G>T
|
ENSP00000383365.1:p.Asp310Tyr
|
|
ENST00000400525.6:c.859G>T
|
ENSP00000383369.3:p.Asp287Tyr
|
|
ENST00000474308.5:c.871G>T
|
ENSP00000485665.1:p.Asp291Tyr
|
|
ENST00000475995.3:c.425G>T
|
|
|
ENST00000491939.6:c.832G>T
|
ENSP00000485543.1:p.Asp278Tyr
|
|
ENST00000494454.5:n.1002G>T
|
|
|
ENST00000542719.6:c.640G>T
|
ENSP00000485128.2:p.Asp214Tyr
|
|
ENST00000634537.1:c.157G>T
|
ENSP00000489208.1:p.Asp53Tyr
|
|
ENST00000635155.1:n.514G>T
|
|
|
NM_001282512.1:c.928G>T
|
NP_001269441.1:p.Asp310Tyr
|
|
NM_006440.4:c.928G>T
|
NP_006431.2:p.Asp310Tyr
|
|
NM_001282512.2:c.928G>T
|
NP_001269441.1:p.Asp310Tyr
|
|
NM_001352300.1:c.925G>T
|
NP_001339229.1:p.Asp309Tyr
|
|
NM_001352301.1:c.838G>T
|
NP_001339230.1:p.Asp280Tyr
|
|
NM_001352302.1:c.640G>T
|
NP_001339231.1:p.Asp214Tyr
|
|
NM_001352303.1:c.832G>T
|
NP_001339232.1:p.Asp278Tyr
|
|
NR_147957.1:n.1060G>T
|
|
|
NM_006440.5:c.928G>T
MANE Select
|
NP_006431.2:p.Asp310Tyr
|
|
NM_001282512.3:c.928G>T
|
NP_001269441.1:p.Asp310Tyr
|
|
NM_001352300.2:c.925G>T
|
NP_001339229.1:p.Asp309Tyr
|
|
NR_147957.2:n.886G>T
|
|
|
NM_001352301.2:c.838G>T
|
NP_001339230.1:p.Asp280Tyr
|
|
NM_001352302.2:c.640G>T
|
NP_001339231.1:p.Asp214Tyr
|
|
NM_001352303.2:c.832G>T
|
NP_001339232.1:p.Asp278Tyr
|
|