ENST00000405392.6:c.2794A>T
|
ENSP00000384484.2:p.Asn932Tyr
|
|
ENST00000679454.1:c.2791A>T
MANE Select
|
ENSP00000505261.1:p.Asn931Tyr
|
|
ENST00000260600.9:c.2791A>T
|
ENSP00000260600.5:p.Asn931Tyr
|
|
ENST00000405392.5:c.2794A>T
|
ENSP00000384484.2:p.Asn932Tyr
|
|
ENST00000485887.1:n.63A>T
|
|
|
ENST00000606682.5:c.1732A>T
|
ENSP00000475652.1:p.Asn578Tyr
|
|
NM_004036.3:c.2791A>T
|
NP_004027.2:p.Asn931Tyr
|
|
XM_005264104.1:c.2794A>T
|
XP_005264161.1:p.Asn932Tyr
|
|
XM_005264105.1:c.2791A>T
|
XP_005264162.1:p.Asn931Tyr
|
|
XM_006711925.1:c.2860A>T
|
XP_006711988.1:p.Asn954Tyr
|
|
XM_011532489.1:c.2917A>T
|
XP_011530791.1:p.Asn973Tyr
|
|
XM_011532490.1:c.2914A>T
|
XP_011530792.1:p.Asn972Tyr
|
|
XM_011532491.1:c.2851A>T
|
XP_011530793.1:p.Asn951Tyr
|
|
XM_011532492.1:c.2917A>T
|
XP_011530794.1:p.Asn973Tyr
|
|
XM_011532493.1:c.2779A>T
|
XP_011530795.1:p.Asn927Tyr
|
|
XM_011532494.1:c.2719A>T
|
XP_011530796.1:p.Asn907Tyr
|
|
XM_011532495.1:c.2251A>T
|
XP_011530797.1:p.Asn751Tyr
|
|
XM_011532496.1:c.2194A>T
|
XP_011530798.1:p.Asn732Tyr
|
|
NM_001320613.1:c.2794A>T
|
NP_001307542.1:p.Asn932Tyr
|
|
NM_004036.4:c.2791A>T
|
NP_004027.2:p.Asn931Tyr
|
|
XM_011532492.2:c.2917A>T
|
XP_011530794.1:p.Asn973Tyr
|
|
XM_017003186.1:c.2857A>T
|
XP_016858675.1:p.Asn953Tyr
|
|
XM_017003187.1:c.2848A>T
|
XP_016858676.1:p.Asn950Tyr
|
|
XM_017003188.1:c.2914A>T
|
XP_016858677.1:p.Asn972Tyr
|
|
XM_017003189.1:c.2776A>T
|
XP_016858678.1:p.Asn926Tyr
|
|
XM_017003190.1:c.2653A>T
|
XP_016858679.1:p.Asn885Tyr
|
|
XM_017003191.1:c.2281A>T
|
XP_016858680.1:p.Asn761Tyr
|
|
XM_017003192.1:c.2071A>T
|
XP_016858681.1:p.Asn691Tyr
|
|
XM_017003193.1:c.2068A>T
|
XP_016858682.1:p.Asn690Tyr
|
|
NM_001320613.2:c.2794A>T
|
NP_001307542.1:p.Asn932Tyr
|
|
NM_001377128.1:c.2857A>T
|
NP_001364057.1:p.Asn953Tyr
|
|
NM_001377129.1:c.2653A>T
|
NP_001364058.1:p.Asn885Tyr
|
|
NM_001377130.1:c.2332-671A>T
|
NP_001364059.1:n.2332-671A>T
|
|
NM_001377131.1:c.2068A>T
|
NP_001364060.1:p.Asn690Tyr
|
|
NM_001377132.1:c.2791A>T
|
NP_001364061.1:p.Asn931Tyr
|
|
NM_004036.5:c.2791A>T
MANE Select
|
NP_004027.2:p.Asn931Tyr
|
|