ENST00000383788.10:c.638G>A
MANE Select
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ENSP00000373298.3:p.Gly213Asp
|
|
ENST00000604401.2:n.634G>A
|
|
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ENST00000679838.1:c.*400G>A
|
ENSP00000505708.1:n.*400G>A
|
|
ENST00000680545.1:n.404G>A
|
|
|
ENST00000681097.1:c.638G>A
|
ENSP00000505397.1:p.Gly213Asp
|
|
ENST00000383781.8:c.608G>A
|
ENSP00000373291.3:p.Gly203Asp
|
|
ENST00000383786.9:c.536G>A
|
ENSP00000373296.3:p.Gly179Asp
|
|
ENST00000383788.9:c.638G>A
|
ENSP00000373298.3:p.Gly213Asp
|
|
ENST00000603808.5:c.638G>A
|
ENSP00000474271.1:p.Gly213Asp
|
|
ENST00000605797.1:c.467G>A
|
ENSP00000474936.1:p.Gly156Asp
|
|
NM_005677.3:c.638G>A
|
NP_005668.2:p.Gly213Asp
|
|
NM_080538.2:c.608G>A
|
NP_536799.1:p.Gly203Asp
|
|
NM_080539.3:c.536G>A
|
NP_536800.2:p.Gly179Asp
|
|
NM_005677.4:c.638G>A
MANE Select
|
NP_005668.2:p.Gly213Asp
|
|
NM_080539.4:c.536G>A
|
NP_536800.2:p.Gly179Asp
|
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