ENST00000405392.6:c.2660_2661delinsGC
|
ENSP00000384484.2:p.Arg887=
|
|
ENST00000679454.1:c.2657_2658delinsGC
MANE Select
|
ENSP00000505261.1:p.Arg886=
|
|
ENST00000260600.9:c.2657_2658delinsGC
|
ENSP00000260600.5:p.Arg886=
|
|
ENST00000405392.5:c.2660_2661delinsGC
|
ENSP00000384484.2:p.Arg887=
|
|
ENST00000606682.5:c.1598_1599delinsGC
|
ENSP00000475652.1:p.Arg533=
|
|
NM_004036.3:c.2657_2658delinsGC
|
NP_004027.2:p.Arg886=
|
|
XM_005264104.1:c.2660_2661delinsGC
|
XP_005264161.1:p.Arg887=
|
|
XM_005264105.1:c.2657_2658delinsGC
|
XP_005264162.1:p.Arg886=
|
|
XM_006711925.1:c.2726_2727delinsGC
|
XP_006711988.1:p.Arg909=
|
|
XM_011532489.1:c.2783_2784delinsGC
|
XP_011530791.1:p.Arg928=
|
|
XM_011532490.1:c.2780_2781delinsGC
|
XP_011530792.1:p.Arg927=
|
|
XM_011532491.1:c.2717_2718delinsGC
|
XP_011530793.1:p.Arg906=
|
|
XM_011532492.1:c.2783_2784delinsGC
|
XP_011530794.1:p.Arg928=
|
|
XM_011532493.1:c.2645_2646delinsGC
|
XP_011530795.1:p.Arg882=
|
|
XM_011532494.1:c.2585_2586delinsGC
|
XP_011530796.1:p.Arg862=
|
|
XM_011532495.1:c.2117_2118delinsGC
|
XP_011530797.1:p.Arg706=
|
|
XM_011532496.1:c.2060_2061delinsGC
|
XP_011530798.1:p.Arg687=
|
|
NM_001320613.1:c.2660_2661delinsGC
|
NP_001307542.1:p.Arg887=
|
|
NM_004036.4:c.2657_2658delinsGC
|
NP_004027.2:p.Arg886=
|
|
XM_011532492.2:c.2783_2784delinsGC
|
XP_011530794.1:p.Arg928=
|
|
XM_017003186.1:c.2723_2724delinsGC
|
XP_016858675.1:p.Arg908=
|
|
XM_017003187.1:c.2714_2715delinsGC
|
XP_016858676.1:p.Arg905=
|
|
XM_017003188.1:c.2780_2781delinsGC
|
XP_016858677.1:p.Arg927=
|
|
XM_017003189.1:c.2642_2643delinsGC
|
XP_016858678.1:p.Arg881=
|
|
XM_017003190.1:c.2519_2520delinsGC
|
XP_016858679.1:p.Arg840=
|
|
XM_017003191.1:c.2147_2148delinsGC
|
XP_016858680.1:p.Arg716=
|
|
XM_017003192.1:c.1937_1938delinsGC
|
XP_016858681.1:p.Arg646=
|
|
XM_017003193.1:c.1934_1935delinsGC
|
XP_016858682.1:p.Arg645=
|
|
NM_001320613.2:c.2660_2661delinsGC
|
NP_001307542.1:p.Arg887=
|
|
NM_001377128.1:c.2723_2724delinsGC
|
NP_001364057.1:p.Arg908=
|
|
NM_001377129.1:c.2519_2520delinsGC
|
NP_001364058.1:p.Arg840=
|
|
NM_001377130.1:c.2252_2253delinsGC
|
NP_001364059.1:p.Arg751=
|
|
NM_001377131.1:c.1934_1935delinsGC
|
NP_001364060.1:p.Arg645=
|
|
NM_001377132.1:c.2657_2658delinsGC
|
NP_001364061.1:p.Arg886=
|
|
NM_004036.5:c.2657_2658delinsGC
MANE Select
|
NP_004027.2:p.Arg886=
|
|