ENST00000474887.6:c.960_961delinsCG
|
|
|
ENST00000683393.1:c.1857_1858delinsCG
|
ENSP00000508654.1:n.1857_1858delinsCG
|
|
ENST00000683760.1:c.2042_2043delinsCG
|
ENSP00000507765.1:p.Pro681=
|
|
ENST00000321117.10:c.2711_2712delinsCG
MANE Select
|
ENSP00000324375.5:p.Pro904=
|
|
ENST00000264709.7:c.2711_2712delinsCG
|
ENSP00000264709.3:p.Pro904=
|
|
ENST00000321117.9:c.2711_2712delinsCG
|
ENSP00000324375.5:p.Pro904=
|
|
ENST00000380746.8:c.2144_2145delinsCG
|
ENSP00000370122.4:p.Pro715=
|
|
ENST00000380756.7:c.*564_*565delinsCG
|
ENSP00000370132.3:n.*564_*565delinsCG
|
|
ENST00000402667.1:c.2042_2043delinsCG
|
ENSP00000384237.1:p.Pro681=
|
|
NM_022552.4:c.2711_2712delinsCG , LRG_459t1:c.2711_2712delinsCG
|
NP_072046.2:p.Pro904=
|
|
NM_153759.3:c.2144_2145delinsCG , LRG_459t2:c.2144_2145delinsCG
|
NP_715640.2:p.Pro715=
|
|
NM_175629.2:c.2711_2712delinsCG , LRG_459t4:c.2711_2712delinsCG
|
NP_783328.1:p.Pro904=
|
|
XM_005264175.3:c.2711_2712delinsCG
|
XP_005264232.1:p.Pro904=
|
|
XM_005264177.3:c.2042_2043delinsCG
|
XP_005264234.1:p.Pro681=
|
|
XM_006711958.2:c.2267_2268delinsCG
|
XP_006712021.1:p.Pro756=
|
|
XM_011532662.1:c.2564_2565delinsCG
|
XP_011530964.1:p.Pro855=
|
|
XM_011532663.1:c.2546_2547delinsCG
|
XP_011530965.1:p.Pro849=
|
|
XM_011532665.1:c.2255_2256delinsCG
|
XP_011530967.1:p.Pro752=
|
|
XM_011532666.1:c.2183_2184delinsCG
|
XP_011530968.1:p.Pro728=
|
|
XM_011532667.1:c.2042_2043delinsCG
|
XP_011530969.1:p.Pro681=
|
|
NM_001320893.1:c.2255_2256delinsCG
|
NP_001307822.1:p.Pro752=
|
|
NR_135490.1:n.3248_3249delinsCG
|
|
|
XM_005264175.5:c.2711_2712delinsCG
|
XP_005264232.1:p.Pro904=
|
|
XM_005264177.4:c.2042_2043delinsCG
|
XP_005264234.1:p.Pro681=
|
|
XM_011532662.2:c.2564_2565delinsCG
|
XP_011530964.1:p.Pro855=
|
|
XM_011532663.2:c.2546_2547delinsCG
|
XP_011530965.1:p.Pro849=
|
|
XM_011532666.2:c.2183_2184delinsCG
|
XP_011530968.1:p.Pro728=
|
|
XM_011532667.3:c.2042_2043delinsCG
|
XP_011530969.1:p.Pro681=
|
|
XM_017003526.1:c.2711_2712delinsCG
|
XP_016859015.1:p.Pro904=
|
|
XM_017003527.1:c.2042_2043delinsCG
|
XP_016859016.1:p.Pro681=
|
|
XR_001738657.1:n.2918_2919delinsCG
|
|
|
NM_001375819.1:c.2042_2043delinsCG
|
NP_001362748.1:p.Pro681=
|
|
NR_135490.2:n.3141_3142delinsCG
|
|
|
NM_022552.5:c.2711_2712delinsCG
MANE Select
|
NP_072046.2:p.Pro904=
|
|