ENST00000310581.10:c.2234C>A
MANE Select
|
ENSP00000309572.5:p.Ala745Asp
|
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ENST00000656021.1:c.*1780C>A
|
ENSP00000499759.1:n.*1780C>A
|
|
ENST00000310581.9:c.2234C>A
|
ENSP00000309572.5:p.Ala745Asp
|
|
ENST00000334602.10:c.2234C>A
|
ENSP00000334346.6:p.Ala745Asp
|
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ENST00000460137.6:c.2198C>A
|
ENSP00000425003.1:p.Ala733Asp
|
|
ENST00000484238.6:n.1047C>A
|
|
|
ENST00000508104.2:c.2234C>A
|
ENSP00000426042.2:p.Ala745Asp
|
|
NM_001193376.1:c.2234C>A
|
NP_001180305.1:p.Ala745Asp
|
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NM_198253.2:c.2234C>A , LRG_343t1:c.2234C>A
|
NP_937983.2:p.Ala745Asp
|
|
XM_011514104.1:c.704C>A
|
XP_011512406.1:p.Ala235Asp
|
|
XM_011514105.1:c.590C>A
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XP_011512407.1:p.Ala197Asp
|
|
XM_011514106.1:c.590C>A
|
XP_011512408.1:p.Ala197Asp
|
|
NR_149162.1:n.2292C>A
|
|
|
NR_149163.1:n.2256C>A
|
|
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NM_001193376.2:c.2234C>A
|
NP_001180305.1:p.Ala745Asp
|
|
NM_198253.3:c.2234C>A
MANE Select
|
NP_937983.2:p.Ala745Asp
|
|
NR_149162.2:n.2313C>A
|
|
|
NR_149163.2:n.2277C>A
|
|
|
NM_001193376.3:c.2234C>A
|
NP_001180305.1:p.Ala745Asp
|
|
NR_149162.3:n.2313C>A
|
|
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NR_149163.3:n.2277C>A
|
|
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