ENST00000342245.9:c.770G>A
MANE Select
|
ENSP00000340409.4:p.Arg257Lys
|
|
ENST00000342245.8:c.770G>A
|
ENSP00000340409.4:p.Arg257Lys
|
|
ENST00000527275.5:c.767G>A
|
ENSP00000435350.1:p.Arg256Lys
|
|
ENST00000530395.1:c.-50G>A
|
ENSP00000431479.1:n.-50G>A
|
|
ENST00000531303.5:c.438+332G>A
|
ENSP00000432625.1:n.438+332G>A
|
|
ENST00000533123.5:c.770G>A
|
ENSP00000435950.1:p.Arg257Lys
|
|
ENST00000533196.1:n.375-171G>A
|
|
|
ENST00000534405.5:c.770G>A
|
ENSP00000434353.1:p.Arg257Lys
|
|
NM_000543.4:c.770G>A
|
NP_000534.3:p.Arg257Lys
|
|
NM_001007593.2:c.767G>A
|
NP_001007594.2:p.Arg256Lys
|
|
XM_005253075.3:c.770G>A
|
XP_005253132.1:p.Arg257Lys
|
|
XM_011520303.1:c.770G>A
|
XP_011518605.1:p.Arg257Lys
|
|
XM_011520304.1:c.770G>A
|
XP_011518606.1:p.Arg257Lys
|
|
XR_930886.1:n.1068G>A
|
|
|
NM_001318087.1:c.770G>A
|
NP_001305016.1:p.Arg257Lys
|
|
NM_001318088.1:c.-192G>A
|
NP_001305017.1:n.-192G>A
|
|
NM_001365135.1:c.770G>A
|
NP_001352064.1:p.Arg257Lys
|
|
NR_027400.2:n.955G>A
|
|
|
NR_134502.1:n.623+332G>A
|
|
|
XM_011520304.2:c.770G>A
|
XP_011518606.1:p.Arg257Lys
|
|
XR_001747940.2:n.895G>A
|
|
|
XR_002957158.1:n.895G>A
|
|
|
NM_000543.5:c.770G>A
MANE Select
|
NP_000534.3:p.Arg257Lys
|
|
NM_001007593.3:c.767G>A
|
NP_001007594.2:p.Arg256Lys
|
|
NM_001318087.2:c.770G>A
|
NP_001305016.1:p.Arg257Lys
|
|
NM_001318088.2:c.-192G>A
|
NP_001305017.1:n.-192G>A
|
|
NM_001365135.2:c.770G>A
|
NP_001352064.1:p.Arg257Lys
|
|
NR_027400.3:n.895G>A
|
|
|
NR_134502.2:n.563+332G>A
|
|
|