ENST00000405392.6:c.2758T>C
|
ENSP00000384484.2:p.Tyr920His
|
|
ENST00000679454.1:c.2755T>C
MANE Select
|
ENSP00000505261.1:p.Tyr919His
|
|
ENST00000260600.9:c.2755T>C
|
ENSP00000260600.5:p.Tyr919His
|
|
ENST00000405392.5:c.2758T>C
|
ENSP00000384484.2:p.Tyr920His
|
|
ENST00000485887.1:n.27T>C
|
|
|
ENST00000606682.5:c.1696T>C
|
ENSP00000475652.1:p.Tyr566His
|
|
NM_004036.3:c.2755T>C
|
NP_004027.2:p.Tyr919His
|
|
XM_005264104.1:c.2758T>C
|
XP_005264161.1:p.Tyr920His
|
|
XM_005264105.1:c.2755T>C
|
XP_005264162.1:p.Tyr919His
|
|
XM_006711925.1:c.2824T>C
|
XP_006711988.1:p.Tyr942His
|
|
XM_011532489.1:c.2881T>C
|
XP_011530791.1:p.Tyr961His
|
|
XM_011532490.1:c.2878T>C
|
XP_011530792.1:p.Tyr960His
|
|
XM_011532491.1:c.2815T>C
|
XP_011530793.1:p.Tyr939His
|
|
XM_011532492.1:c.2881T>C
|
XP_011530794.1:p.Tyr961His
|
|
XM_011532493.1:c.2743T>C
|
XP_011530795.1:p.Tyr915His
|
|
XM_011532494.1:c.2683T>C
|
XP_011530796.1:p.Tyr895His
|
|
XM_011532495.1:c.2215T>C
|
XP_011530797.1:p.Tyr739His
|
|
XM_011532496.1:c.2158T>C
|
XP_011530798.1:p.Tyr720His
|
|
NM_001320613.1:c.2758T>C
|
NP_001307542.1:p.Tyr920His
|
|
NM_004036.4:c.2755T>C
|
NP_004027.2:p.Tyr919His
|
|
XM_011532492.2:c.2881T>C
|
XP_011530794.1:p.Tyr961His
|
|
XM_017003186.1:c.2821T>C
|
XP_016858675.1:p.Tyr941His
|
|
XM_017003187.1:c.2812T>C
|
XP_016858676.1:p.Tyr938His
|
|
XM_017003188.1:c.2878T>C
|
XP_016858677.1:p.Tyr960His
|
|
XM_017003189.1:c.2740T>C
|
XP_016858678.1:p.Tyr914His
|
|
XM_017003190.1:c.2617T>C
|
XP_016858679.1:p.Tyr873His
|
|
XM_017003191.1:c.2245T>C
|
XP_016858680.1:p.Tyr749His
|
|
XM_017003192.1:c.2035T>C
|
XP_016858681.1:p.Tyr679His
|
|
XM_017003193.1:c.2032T>C
|
XP_016858682.1:p.Tyr678His
|
|
NM_001320613.2:c.2758T>C
|
NP_001307542.1:p.Tyr920His
|
|
NM_001377128.1:c.2821T>C
|
NP_001364057.1:p.Tyr941His
|
|
NM_001377129.1:c.2617T>C
|
NP_001364058.1:p.Tyr873His
|
|
NM_001377130.1:c.2332-707T>C
|
NP_001364059.1:n.2332-707T>C
|
|
NM_001377131.1:c.2032T>C
|
NP_001364060.1:p.Tyr678His
|
|
NM_001377132.1:c.2755T>C
|
NP_001364061.1:p.Tyr919His
|
|
NM_004036.5:c.2755T>C
MANE Select
|
NP_004027.2:p.Tyr919His
|
|