ENST00000370096.9:c.3140A>T
MANE Select
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ENSP00000359114.3:p.Glu1047Val
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ENST00000353414.8:c.3023A>T
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ENSP00000302551.6:p.Glu1008Val
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ENST00000358392.6:c.3176A>T
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ENSP00000351163.2:p.Glu1059Val
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ENST00000370096.7:c.3140A>T
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ENSP00000359114.3:p.Glu1047Val
|
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ENST00000465209.1:n.148A>T
|
|
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ENST00000512756.5:c.2792A>T
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ENSP00000426533.1:p.Glu931Val
|
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ENST00000635193.1:c.2474A>T
|
|
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NM_001190709.1:c.3023A>T
|
NP_001177638.1:p.Glu1008Val
|
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NM_001854.3:c.3140A>T
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NP_001845.3:p.Glu1047Val
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NM_080629.2:c.3176A>T
|
NP_542196.2:p.Glu1059Val
|
|
NM_080630.3:c.2792A>T
|
NP_542197.3:p.Glu931Val
|
|
XM_011540719.1:c.3140A>T
|
XP_011539021.1:p.Glu1047Val
|
|
XM_011540720.1:c.1373A>T
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XP_011539022.1:p.Glu458Val
|
|
XM_011540721.1:c.728A>T
|
XP_011539023.1:p.Glu243Val
|
|
NR_134980.1:n.3474A>T
|
|
|
XM_017000334.1:c.3293A>T
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XP_016855823.1:p.Glu1098Val
|
|
XM_017000335.1:c.3287A>T
|
XP_016855824.1:p.Glu1096Val
|
|
XM_017000336.1:c.3293A>T
|
XP_016855825.1:p.Glu1098Val
|
|
XM_017000337.1:c.1691A>T
|
XP_016855826.1:p.Glu564Val
|
|
NM_001854.4:c.3140A>T
MANE Select
|
NP_001845.3:p.Glu1047Val
|
|
NM_080630.4:c.2792A>T
|
NP_542197.3:p.Glu931Val
|
|
NR_134980.2:n.3500A>T
|
|
|
NM_001190709.2:c.3023A>T
|
NP_001177638.1:p.Glu1008Val
|
|
NM_080629.3:c.3176A>T
|
NP_542196.2:p.Glu1059Val
|
|