ENST00000405392.6:c.2762A>T
|
ENSP00000384484.2:p.Asp921Val
|
|
ENST00000679454.1:c.2759A>T
MANE Select
|
ENSP00000505261.1:p.Asp920Val
|
|
ENST00000260600.9:c.2759A>T
|
ENSP00000260600.5:p.Asp920Val
|
|
ENST00000405392.5:c.2762A>T
|
ENSP00000384484.2:p.Asp921Val
|
|
ENST00000485887.1:n.31A>T
|
|
|
ENST00000606682.5:c.1700A>T
|
ENSP00000475652.1:p.Asp567Val
|
|
NM_004036.3:c.2759A>T
|
NP_004027.2:p.Asp920Val
|
|
XM_005264104.1:c.2762A>T
|
XP_005264161.1:p.Asp921Val
|
|
XM_005264105.1:c.2759A>T
|
XP_005264162.1:p.Asp920Val
|
|
XM_006711925.1:c.2828A>T
|
XP_006711988.1:p.Asp943Val
|
|
XM_011532489.1:c.2885A>T
|
XP_011530791.1:p.Asp962Val
|
|
XM_011532490.1:c.2882A>T
|
XP_011530792.1:p.Asp961Val
|
|
XM_011532491.1:c.2819A>T
|
XP_011530793.1:p.Asp940Val
|
|
XM_011532492.1:c.2885A>T
|
XP_011530794.1:p.Asp962Val
|
|
XM_011532493.1:c.2747A>T
|
XP_011530795.1:p.Asp916Val
|
|
XM_011532494.1:c.2687A>T
|
XP_011530796.1:p.Asp896Val
|
|
XM_011532495.1:c.2219A>T
|
XP_011530797.1:p.Asp740Val
|
|
XM_011532496.1:c.2162A>T
|
XP_011530798.1:p.Asp721Val
|
|
NM_001320613.1:c.2762A>T
|
NP_001307542.1:p.Asp921Val
|
|
NM_004036.4:c.2759A>T
|
NP_004027.2:p.Asp920Val
|
|
XM_011532492.2:c.2885A>T
|
XP_011530794.1:p.Asp962Val
|
|
XM_017003186.1:c.2825A>T
|
XP_016858675.1:p.Asp942Val
|
|
XM_017003187.1:c.2816A>T
|
XP_016858676.1:p.Asp939Val
|
|
XM_017003188.1:c.2882A>T
|
XP_016858677.1:p.Asp961Val
|
|
XM_017003189.1:c.2744A>T
|
XP_016858678.1:p.Asp915Val
|
|
XM_017003190.1:c.2621A>T
|
XP_016858679.1:p.Asp874Val
|
|
XM_017003191.1:c.2249A>T
|
XP_016858680.1:p.Asp750Val
|
|
XM_017003192.1:c.2039A>T
|
XP_016858681.1:p.Asp680Val
|
|
XM_017003193.1:c.2036A>T
|
XP_016858682.1:p.Asp679Val
|
|
NM_001320613.2:c.2762A>T
|
NP_001307542.1:p.Asp921Val
|
|
NM_001377128.1:c.2825A>T
|
NP_001364057.1:p.Asp942Val
|
|
NM_001377129.1:c.2621A>T
|
NP_001364058.1:p.Asp874Val
|
|
NM_001377130.1:c.2332-703A>T
|
NP_001364059.1:n.2332-703A>T
|
|
NM_001377131.1:c.2036A>T
|
NP_001364060.1:p.Asp679Val
|
|
NM_001377132.1:c.2759A>T
|
NP_001364061.1:p.Asp920Val
|
|
NM_004036.5:c.2759A>T
MANE Select
|
NP_004027.2:p.Asp920Val
|
|