ENST00000310581.10:c.1978G=
MANE Select
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ENSP00000309572.5:p.Ala660=
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ENST00000656021.1:c.*1524G=
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ENSP00000499759.1:n.*1524G=
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ENST00000310581.9:c.1978G=
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ENSP00000309572.5:p.Ala660=
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ENST00000334602.10:c.1978G=
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ENSP00000334346.6:p.Ala660=
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ENST00000460137.6:c.1978G=
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ENSP00000425003.1:p.Ala660=
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ENST00000484238.6:n.791G=
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|
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ENST00000508104.2:c.1978G=
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ENSP00000426042.2:p.Ala660=
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NM_001193376.1:c.1978G=
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NP_001180305.1:p.Ala660=
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NM_198253.2:c.1978G= , LRG_343t1:c.1978G=
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NP_937983.2:p.Ala660=
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XM_011514104.1:c.448G=
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XP_011512406.1:p.Ala150=
|
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XM_011514105.1:c.334G=
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XP_011512407.1:p.Ala112=
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XM_011514106.1:c.334G=
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XP_011512408.1:p.Ala112=
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NR_149162.1:n.2036G=
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|
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NR_149163.1:n.2036G=
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|
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NM_001193376.2:c.1978G=
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NP_001180305.1:p.Ala660=
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|
NM_198253.3:c.1978G=
MANE Select
|
NP_937983.2:p.Ala660=
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|
NR_149162.2:n.2057G=
|
|
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NR_149163.2:n.2057G=
|
|
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NM_001193376.3:c.1978G=
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NP_001180305.1:p.Ala660=
|
|
NR_149162.3:n.2057G=
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|
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NR_149163.3:n.2057G=
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