ENST00000310581.10:c.3303G>A
MANE Select
|
ENSP00000309572.5:p.Thr1101=
|
|
ENST00000656021.1:c.*2849G>A
|
ENSP00000499759.1:n.*2849G>A
|
|
ENST00000310581.9:c.3303G>A
|
ENSP00000309572.5:p.Thr1101=
|
|
ENST00000334602.10:c.3114G>A
|
ENSP00000334346.6:p.Thr1038=
|
|
ENST00000460137.6:c.2896G>A
|
ENSP00000425003.1:n.2896G>A
|
|
ENST00000484238.6:n.1745G>A
|
|
|
NM_001193376.1:c.3114G>A
|
NP_001180305.1:p.Thr1038=
|
|
NM_198253.2:c.3303G>A , LRG_343t1:c.3303G>A
|
NP_937983.2:p.Thr1101=
|
|
XM_011514104.1:c.1773G>A
|
XP_011512406.1:p.Thr591=
|
|
XM_011514105.1:c.1659G>A
|
XP_011512407.1:p.Thr553=
|
|
XM_011514106.1:c.1659G>A
|
XP_011512408.1:p.Thr553=
|
|
XR_925683.1:n.287-850C>T
|
|
|
NR_149162.1:n.2990G>A
|
|
|
NR_149163.1:n.2954G>A
|
|
|
NM_001193376.2:c.3114G>A
|
NP_001180305.1:p.Thr1038=
|
|
NM_198253.3:c.3303G>A
MANE Select
|
NP_937983.2:p.Thr1101=
|
|
NR_149162.2:n.3011G>A
|
|
|
NR_149163.2:n.2975G>A
|
|
|
NM_001193376.3:c.3114G>A
|
NP_001180305.1:p.Thr1038=
|
|
NR_149162.3:n.3011G>A
|
|
|
NR_149163.3:n.2975G>A
|
|
|