ENST00000405392.6:c.2760T>G
|
ENSP00000384484.2:p.Tyr920Ter
|
|
ENST00000679454.1:c.2757T>G
MANE Select
|
ENSP00000505261.1:p.Tyr919Ter
|
|
ENST00000260600.9:c.2757T>G
|
ENSP00000260600.5:p.Tyr919Ter
|
|
ENST00000405392.5:c.2760T>G
|
ENSP00000384484.2:p.Tyr920Ter
|
|
ENST00000485887.1:n.29T>G
|
|
|
ENST00000606682.5:c.1698T>G
|
ENSP00000475652.1:p.Tyr566Ter
|
|
NM_004036.3:c.2757T>G
|
NP_004027.2:p.Tyr919Ter
|
|
XM_005264104.1:c.2760T>G
|
XP_005264161.1:p.Tyr920Ter
|
|
XM_005264105.1:c.2757T>G
|
XP_005264162.1:p.Tyr919Ter
|
|
XM_006711925.1:c.2826T>G
|
XP_006711988.1:p.Tyr942Ter
|
|
XM_011532489.1:c.2883T>G
|
XP_011530791.1:p.Tyr961Ter
|
|
XM_011532490.1:c.2880T>G
|
XP_011530792.1:p.Tyr960Ter
|
|
XM_011532491.1:c.2817T>G
|
XP_011530793.1:p.Tyr939Ter
|
|
XM_011532492.1:c.2883T>G
|
XP_011530794.1:p.Tyr961Ter
|
|
XM_011532493.1:c.2745T>G
|
XP_011530795.1:p.Tyr915Ter
|
|
XM_011532494.1:c.2685T>G
|
XP_011530796.1:p.Tyr895Ter
|
|
XM_011532495.1:c.2217T>G
|
XP_011530797.1:p.Tyr739Ter
|
|
XM_011532496.1:c.2160T>G
|
XP_011530798.1:p.Tyr720Ter
|
|
NM_001320613.1:c.2760T>G
|
NP_001307542.1:p.Tyr920Ter
|
|
NM_004036.4:c.2757T>G
|
NP_004027.2:p.Tyr919Ter
|
|
XM_011532492.2:c.2883T>G
|
XP_011530794.1:p.Tyr961Ter
|
|
XM_017003186.1:c.2823T>G
|
XP_016858675.1:p.Tyr941Ter
|
|
XM_017003187.1:c.2814T>G
|
XP_016858676.1:p.Tyr938Ter
|
|
XM_017003188.1:c.2880T>G
|
XP_016858677.1:p.Tyr960Ter
|
|
XM_017003189.1:c.2742T>G
|
XP_016858678.1:p.Tyr914Ter
|
|
XM_017003190.1:c.2619T>G
|
XP_016858679.1:p.Tyr873Ter
|
|
XM_017003191.1:c.2247T>G
|
XP_016858680.1:p.Tyr749Ter
|
|
XM_017003192.1:c.2037T>G
|
XP_016858681.1:p.Tyr679Ter
|
|
XM_017003193.1:c.2034T>G
|
XP_016858682.1:p.Tyr678Ter
|
|
NM_001320613.2:c.2760T>G
|
NP_001307542.1:p.Tyr920Ter
|
|
NM_001377128.1:c.2823T>G
|
NP_001364057.1:p.Tyr941Ter
|
|
NM_001377129.1:c.2619T>G
|
NP_001364058.1:p.Tyr873Ter
|
|
NM_001377130.1:c.2332-705T>G
|
NP_001364059.1:n.2332-705T>G
|
|
NM_001377131.1:c.2034T>G
|
NP_001364060.1:p.Tyr678Ter
|
|
NM_001377132.1:c.2757T>G
|
NP_001364061.1:p.Tyr919Ter
|
|
NM_004036.5:c.2757T>G
MANE Select
|
NP_004027.2:p.Tyr919Ter
|
|