ENST00000333213.11:c.986G>A
MANE Select
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ENSP00000327487.6:p.Gly329Glu
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ENST00000434205.8:c.683G>A
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ENSP00000406559.4:p.Gly228Glu
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ENST00000545228.3:c.986G>A
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ENSP00000438169.3:p.Gly329Glu
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ENST00000579449.2:n.785G>A
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ENST00000580013.6:n.1189G>A
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ENST00000679370.1:n.1567G>A
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ENST00000679429.1:c.*444G>A
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ENSP00000505403.1:n.*444G>A
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ENST00000679443.1:n.1055G>A
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ENST00000679782.1:c.986G>A
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ENSP00000505995.1:p.Gly329Glu
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ENST00000679919.1:n.1055G>A
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ENST00000679928.1:c.*597G>A
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ENSP00000506071.1:n.*597G>A
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ENST00000680528.1:n.1011G>A
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ENST00000680999.1:c.986G>A
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ENSP00000504984.1:p.Gly329Glu
|
|
ENST00000681282.1:c.*232G>A
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ENSP00000506339.1:n.*232G>A
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ENST00000333213.10:c.986G>A
|
ENSP00000327487.6:p.Gly329Glu
|
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ENST00000545228.2:c.75G>A
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ENST00000578415.1:c.946G>A
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ENST00000583173.5:c.519G>A
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ENSP00000463619.1:p.Trp173Ter
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NM_207346.2:c.986G>A
|
NP_997229.2:p.Gly329Glu
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XM_005257229.2:c.986G>A
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XP_005257286.1:p.Gly329Glu
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XM_006721821.2:c.683G>A
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XP_006721884.1:p.Gly228Glu
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XM_011524616.1:c.986G>A
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XP_011522918.1:p.Gly329Glu
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XM_011524617.1:c.986G>A
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XP_011522919.1:p.Gly329Glu
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XM_011524618.1:c.986G>A
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XP_011522920.1:p.Gly329Glu
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XR_243646.2:n.1016G>A
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XM_005257229.4:c.986G>A
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XP_005257286.1:p.Gly329Glu
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XR_243646.4:n.1022G>A
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NM_207346.3:c.986G>A
MANE Select
|
NP_997229.2:p.Gly329Glu
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