ENST00000310581.10:c.2951G>A
MANE Select
|
ENSP00000309572.5:p.Ser984Asn
|
|
ENST00000656021.1:c.*2497G>A
|
ENSP00000499759.1:n.*2497G>A
|
|
ENST00000667927.1:n.239G>A
|
|
|
ENST00000310581.9:c.2951G>A
|
ENSP00000309572.5:p.Ser984Asn
|
|
ENST00000334602.10:c.2762G>A
|
ENSP00000334346.6:p.Ser921Asn
|
|
ENST00000460137.6:c.2544G>A
|
ENSP00000425003.1:n.2544G>A
|
|
ENST00000484238.6:n.1393G>A
|
|
|
NM_001193376.1:c.2762G>A
|
NP_001180305.1:p.Ser921Asn
|
|
NM_198253.2:c.2951G>A , LRG_343t1:c.2951G>A
|
NP_937983.2:p.Ser984Asn
|
|
XM_011514104.1:c.1421G>A
|
XP_011512406.1:p.Ser474Asn
|
|
XM_011514105.1:c.1307G>A
|
XP_011512407.1:p.Ser436Asn
|
|
XM_011514106.1:c.1307G>A
|
XP_011512408.1:p.Ser436Asn
|
|
NR_149162.1:n.2638G>A
|
|
|
NR_149163.1:n.2602G>A
|
|
|
NM_001193376.2:c.2762G>A
|
NP_001180305.1:p.Ser921Asn
|
|
NM_198253.3:c.2951G>A
MANE Select
|
NP_937983.2:p.Ser984Asn
|
|
NR_149162.2:n.2659G>A
|
|
|
NR_149163.2:n.2623G>A
|
|
|
NM_001193376.3:c.2762G>A
|
NP_001180305.1:p.Ser921Asn
|
|
NR_149162.3:n.2659G>A
|
|
|
NR_149163.3:n.2623G>A
|
|
|