ENST00000636937.2:c.3343G>A
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ENSP00000516154.1:p.Ala1115Thr
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ENST00000268124.11:c.3343G>A
MANE Select
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ENSP00000268124.5:p.Ala1115Thr
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ENST00000530292.3:c.2944G>A
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ENSP00000432885.2:p.Ala982Thr
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ENST00000635986.2:c.*413G>A
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ENSP00000490653.2:n.*413G>A
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ENST00000636774.1:c.*1910G>A
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ENSP00000489799.1:n.*1910G>A
|
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ENST00000637238.1:c.2152G>A
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ENSP00000490756.1:n.2152G>A
|
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ENST00000637264.1:c.2415G>A
|
|
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ENST00000666746.1:c.2920G>A
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|
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ENST00000672071.1:n.3541G>A
|
|
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ENST00000672695.1:n.520G>A
|
|
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ENST00000672923.2:n.3343G>A
|
|
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ENST00000268124.9:c.3343G>A
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ENSP00000268124.5:p.Ala1115Thr
|
|
ENST00000442287.6:c.3343G>A
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ENSP00000399851.2:p.Ala1115Thr
|
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ENST00000530292.2:c.427G>A
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ENSP00000432885.1:p.Ala143Thr
|
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ENST00000631044.2:c.*2767G>A
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ENSP00000486730.1:n.*2767G>A
|
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NM_001126131.1:c.3343G>A
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NP_001119603.1:p.Ala1115Thr
|
|
NM_002693.2:c.3343G>A
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NP_002684.1:p.Ala1115Thr
|
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NM_001126131.2:c.3343G>A
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NP_001119603.1:p.Ala1115Thr
|
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NM_002693.3:c.3343G>A
MANE Select
|
NP_002684.1:p.Ala1115Thr
|
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