ENST00000405392.6:c.2763_2766delinsTGAG
|
ENSP00000384484.2:p.Asp921=
|
|
ENST00000679454.1:c.2760_2763delinsTGAG
MANE Select
|
ENSP00000505261.1:p.Asp920=
|
|
ENST00000260600.9:c.2760_2763delinsTGAG
|
ENSP00000260600.5:p.Asp920=
|
|
ENST00000405392.5:c.2763_2766delinsTGAG
|
ENSP00000384484.2:p.Asp921=
|
|
ENST00000485887.1:n.32_35delinsTGAG
|
|
|
ENST00000606682.5:c.1701_1704delinsTGAG
|
ENSP00000475652.1:p.Asp567=
|
|
NM_004036.3:c.2760_2763delinsTGAG
|
NP_004027.2:p.Asp920=
|
|
XM_005264104.1:c.2763_2766delinsTGAG
|
XP_005264161.1:p.Asp921=
|
|
XM_005264105.1:c.2760_2763delinsTGAG
|
XP_005264162.1:p.Asp920=
|
|
XM_006711925.1:c.2829_2832delinsTGAG
|
XP_006711988.1:p.Asp943=
|
|
XM_011532489.1:c.2886_2889delinsTGAG
|
XP_011530791.1:p.Asp962=
|
|
XM_011532490.1:c.2883_2886delinsTGAG
|
XP_011530792.1:p.Asp961=
|
|
XM_011532491.1:c.2820_2823delinsTGAG
|
XP_011530793.1:p.Asp940=
|
|
XM_011532492.1:c.2886_2889delinsTGAG
|
XP_011530794.1:p.Asp962=
|
|
XM_011532493.1:c.2748_2751delinsTGAG
|
XP_011530795.1:p.Asp916=
|
|
XM_011532494.1:c.2688_2691delinsTGAG
|
XP_011530796.1:p.Asp896=
|
|
XM_011532495.1:c.2220_2223delinsTGAG
|
XP_011530797.1:p.Asp740=
|
|
XM_011532496.1:c.2163_2166delinsTGAG
|
XP_011530798.1:p.Asp721=
|
|
NM_001320613.1:c.2763_2766delinsTGAG
|
NP_001307542.1:p.Asp921=
|
|
NM_004036.4:c.2760_2763delinsTGAG
|
NP_004027.2:p.Asp920=
|
|
XM_011532492.2:c.2886_2889delinsTGAG
|
XP_011530794.1:p.Asp962=
|
|
XM_017003186.1:c.2826_2829delinsTGAG
|
XP_016858675.1:p.Asp942=
|
|
XM_017003187.1:c.2817_2820delinsTGAG
|
XP_016858676.1:p.Asp939=
|
|
XM_017003188.1:c.2883_2886delinsTGAG
|
XP_016858677.1:p.Asp961=
|
|
XM_017003189.1:c.2745_2748delinsTGAG
|
XP_016858678.1:p.Asp915=
|
|
XM_017003190.1:c.2622_2625delinsTGAG
|
XP_016858679.1:p.Asp874=
|
|
XM_017003191.1:c.2250_2253delinsTGAG
|
XP_016858680.1:p.Asp750=
|
|
XM_017003192.1:c.2040_2043delinsTGAG
|
XP_016858681.1:p.Asp680=
|
|
XM_017003193.1:c.2037_2040delinsTGAG
|
XP_016858682.1:p.Asp679=
|
|
NM_001320613.2:c.2763_2766delinsTGAG
|
NP_001307542.1:p.Asp921=
|
|
NM_001377128.1:c.2826_2829delinsTGAG
|
NP_001364057.1:p.Asp942=
|
|
NM_001377129.1:c.2622_2625delinsTGAG
|
NP_001364058.1:p.Asp874=
|
|
NM_001377130.1:c.2332-702_2332-699delinsTGAG
|
NP_001364059.1:n.2332-702_2332-699delinsTGAG
|
|
NM_001377131.1:c.2037_2040delinsTGAG
|
NP_001364060.1:p.Asp679=
|
|
NM_001377132.1:c.2760_2763delinsTGAG
|
NP_001364061.1:p.Asp920=
|
|
NM_004036.5:c.2760_2763delinsTGAG
MANE Select
|
NP_004027.2:p.Asp920=
|
|