ENST00000310581.10:c.2930T>G
MANE Select
|
ENSP00000309572.5:p.Val977Gly
|
|
ENST00000656021.1:c.*2476T>G
|
ENSP00000499759.1:n.*2476T>G
|
|
ENST00000667927.1:n.218T>G
|
|
|
ENST00000310581.9:c.2930T>G
|
ENSP00000309572.5:p.Val977Gly
|
|
ENST00000334602.10:c.2741T>G
|
ENSP00000334346.6:p.Val914Gly
|
|
ENST00000460137.6:c.2523T>G
|
ENSP00000425003.1:n.2523T>G
|
|
ENST00000484238.6:n.1372T>G
|
|
|
NM_001193376.1:c.2741T>G
|
NP_001180305.1:p.Val914Gly
|
|
NM_198253.2:c.2930T>G , LRG_343t1:c.2930T>G
|
NP_937983.2:p.Val977Gly
|
|
XM_011514104.1:c.1400T>G
|
XP_011512406.1:p.Val467Gly
|
|
XM_011514105.1:c.1286T>G
|
XP_011512407.1:p.Val429Gly
|
|
XM_011514106.1:c.1286T>G
|
XP_011512408.1:p.Val429Gly
|
|
NR_149162.1:n.2617T>G
|
|
|
NR_149163.1:n.2581T>G
|
|
|
NM_001193376.2:c.2741T>G
|
NP_001180305.1:p.Val914Gly
|
|
NM_198253.3:c.2930T>G
MANE Select
|
NP_937983.2:p.Val977Gly
|
|
NR_149162.2:n.2638T>G
|
|
|
NR_149163.2:n.2602T>G
|
|
|
NM_001193376.3:c.2741T>G
|
NP_001180305.1:p.Val914Gly
|
|
NR_149162.3:n.2638T>G
|
|
|
NR_149163.3:n.2602T>G
|
|
|