ENST00000310581.10:c.2262C=
MANE Select
|
ENSP00000309572.5:p.His754=
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ENST00000656021.1:c.*1808C=
|
ENSP00000499759.1:n.*1808C=
|
|
ENST00000310581.9:c.2262C=
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ENSP00000309572.5:p.His754=
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|
ENST00000334602.10:c.2262C=
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ENSP00000334346.6:p.His754=
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|
ENST00000460137.6:c.2226C=
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ENSP00000425003.1:p.His742=
|
|
ENST00000484238.6:n.1075C=
|
|
|
ENST00000508104.2:c.2262C=
|
ENSP00000426042.2:p.His754=
|
|
NM_001193376.1:c.2262C=
|
NP_001180305.1:p.His754=
|
|
NM_198253.2:c.2262C= , LRG_343t1:c.2262C=
|
NP_937983.2:p.His754=
|
|
XM_011514104.1:c.732C=
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XP_011512406.1:p.His244=
|
|
XM_011514105.1:c.618C=
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XP_011512407.1:p.His206=
|
|
XM_011514106.1:c.618C=
|
XP_011512408.1:p.His206=
|
|
NR_149162.1:n.2320C=
|
|
|
NR_149163.1:n.2284C=
|
|
|
NM_001193376.2:c.2262C=
|
NP_001180305.1:p.His754=
|
|
NM_198253.3:c.2262C=
MANE Select
|
NP_937983.2:p.His754=
|
|
NR_149162.2:n.2341C=
|
|
|
NR_149163.2:n.2305C=
|
|
|
NM_001193376.3:c.2262C=
|
NP_001180305.1:p.His754=
|
|
NR_149162.3:n.2341C=
|
|
|
NR_149163.3:n.2305C=
|
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