ENST00000405392.6:c.2887-262G>A
|
ENSP00000384484.2:n.2887-262G>A
|
|
ENST00000679454.1:c.2884-262G>A
MANE Select
|
ENSP00000505261.1:n.2884-262G>A
|
|
ENST00000260600.9:c.2884-262G>A
|
ENSP00000260600.5:n.2884-262G>A
|
|
ENST00000405392.5:c.2887-262G>A
|
ENSP00000384484.2:n.2887-262G>A
|
|
ENST00000485887.1:n.156-262G>A
|
|
|
ENST00000606682.5:c.1825-262G>A
|
ENSP00000475652.1:n.1825-262G>A
|
|
NM_004036.3:c.2884-262G>A
|
NP_004027.2:n.2884-262G>A
|
|
XM_005264104.1:c.2887-262G>A
|
XP_005264161.1:n.2887-262G>A
|
|
XM_005264105.1:c.2884-262G>A
|
XP_005264162.1:n.2884-262G>A
|
|
XM_006711925.1:c.2953-262G>A
|
XP_006711988.1:n.2953-262G>A
|
|
XM_011532489.1:c.3010-262G>A
|
XP_011530791.1:n.3010-262G>A
|
|
XM_011532490.1:c.3007-262G>A
|
XP_011530792.1:n.3007-262G>A
|
|
XM_011532491.1:c.2944-262G>A
|
XP_011530793.1:n.2944-262G>A
|
|
XM_011532492.1:c.3010-262G>A
|
XP_011530794.1:n.3010-262G>A
|
|
XM_011532493.1:c.2872-262G>A
|
XP_011530795.1:n.2872-262G>A
|
|
XM_011532494.1:c.2812-262G>A
|
XP_011530796.1:n.2812-262G>A
|
|
XM_011532495.1:c.2344-262G>A
|
XP_011530797.1:n.2344-262G>A
|
|
XM_011532496.1:c.2287-262G>A
|
XP_011530798.1:n.2287-262G>A
|
|
NM_001320613.1:c.2887-262G>A
|
NP_001307542.1:n.2887-262G>A
|
|
NM_004036.4:c.2884-262G>A
|
NP_004027.2:n.2884-262G>A
|
|
XM_011532492.2:c.3010-262G>A
|
XP_011530794.1:n.3010-262G>A
|
|
XM_017003186.1:c.2950-262G>A
|
XP_016858675.1:n.2950-262G>A
|
|
XM_017003187.1:c.2941-262G>A
|
XP_016858676.1:n.2941-262G>A
|
|
XM_017003188.1:c.3007-262G>A
|
XP_016858677.1:n.3007-262G>A
|
|
XM_017003189.1:c.2869-262G>A
|
XP_016858678.1:n.2869-262G>A
|
|
XM_017003190.1:c.2746-262G>A
|
XP_016858679.1:n.2746-262G>A
|
|
XM_017003191.1:c.2374-262G>A
|
XP_016858680.1:n.2374-262G>A
|
|
XM_017003192.1:c.2164-262G>A
|
XP_016858681.1:n.2164-262G>A
|
|
XM_017003193.1:c.2161-262G>A
|
XP_016858682.1:n.2161-262G>A
|
|
NM_001320613.2:c.2887-262G>A
|
NP_001307542.1:n.2887-262G>A
|
|
NM_001377128.1:c.2950-262G>A
|
NP_001364057.1:n.2950-262G>A
|
|
NM_001377129.1:c.2746-262G>A
|
NP_001364058.1:n.2746-262G>A
|
|
NM_001377130.1:c.2332-262G>A
|
NP_001364059.1:n.2332-262G>A
|
|
NM_001377131.1:c.2161-262G>A
|
NP_001364060.1:n.2161-262G>A
|
|
NM_001377132.1:c.2884-262G>A
|
NP_001364061.1:n.2884-262G>A
|
|
NM_004036.5:c.2884-262G>A
MANE Select
|
NP_004027.2:n.2884-262G>A
|
|