|
ENST00000310581.10:c.2706G>C
MANE Select
|
ENSP00000309572.5:p.Lys902Asn
|
|
|
ENST00000656021.1:c.*2252G>C
|
ENSP00000499759.1:n.*2252G>C
|
|
|
ENST00000310581.9:c.2706G>C
|
ENSP00000309572.5:p.Lys902Asn
|
|
|
ENST00000334602.10:c.2654+1923G>C
|
ENSP00000334346.6:n.2654+1923G>C
|
|
|
ENST00000460137.6:c.2436+1923G>C
|
ENSP00000425003.1:n.2436+1923G>C
|
|
|
ENST00000484238.6:n.1285+1923G>C
|
|
|
|
ENST00000503656.1:n.113G>C
|
|
|
|
NM_001193376.1:c.2654+1923G>C
|
NP_001180305.1:n.2654+1923G>C
|
|
|
NM_198253.2:c.2706G>C , LRG_343t1:c.2706G>C
|
NP_937983.2:p.Lys902Asn
|
|
|
XM_011514104.1:c.1176G>C
|
XP_011512406.1:p.Lys392Asn
|
|
|
XM_011514105.1:c.1062G>C
|
XP_011512407.1:p.Lys354Asn
|
|
|
XM_011514106.1:c.1062G>C
|
XP_011512408.1:p.Lys354Asn
|
|
|
NR_149162.1:n.2530+1923G>C
|
|
|
|
NR_149163.1:n.2494+1923G>C
|
|
|
|
NM_001193376.2:c.2654+1923G>C
|
NP_001180305.1:n.2654+1923G>C
|
|
|
NM_198253.3:c.2706G>C
MANE Select
|
NP_937983.2:p.Lys902Asn
|
|
|
NR_149162.2:n.2551+1923G>C
|
|
|
|
NR_149163.2:n.2515+1923G>C
|
|
|
|
NM_001193376.3:c.2654+1923G>C
|
NP_001180305.1:n.2654+1923G>C
|
|
|
NR_149162.3:n.2551+1923G>C
|
|
|
|
NR_149163.3:n.2515+1923G>C
|
|
|
