ENST00000405392.6:c.2830A>C
|
ENSP00000384484.2:p.Asn944His
|
|
ENST00000679454.1:c.2827A>C
MANE Select
|
ENSP00000505261.1:p.Asn943His
|
|
ENST00000260600.9:c.2827A>C
|
ENSP00000260600.5:p.Asn943His
|
|
ENST00000405392.5:c.2830A>C
|
ENSP00000384484.2:p.Asn944His
|
|
ENST00000485887.1:n.99A>C
|
|
|
ENST00000606682.5:c.1768A>C
|
ENSP00000475652.1:p.Asn590His
|
|
NM_004036.3:c.2827A>C
|
NP_004027.2:p.Asn943His
|
|
XM_005264104.1:c.2830A>C
|
XP_005264161.1:p.Asn944His
|
|
XM_005264105.1:c.2827A>C
|
XP_005264162.1:p.Asn943His
|
|
XM_006711925.1:c.2896A>C
|
XP_006711988.1:p.Asn966His
|
|
XM_011532489.1:c.2953A>C
|
XP_011530791.1:p.Asn985His
|
|
XM_011532490.1:c.2950A>C
|
XP_011530792.1:p.Asn984His
|
|
XM_011532491.1:c.2887A>C
|
XP_011530793.1:p.Asn963His
|
|
XM_011532492.1:c.2953A>C
|
XP_011530794.1:p.Asn985His
|
|
XM_011532493.1:c.2815A>C
|
XP_011530795.1:p.Asn939His
|
|
XM_011532494.1:c.2755A>C
|
XP_011530796.1:p.Asn919His
|
|
XM_011532495.1:c.2287A>C
|
XP_011530797.1:p.Asn763His
|
|
XM_011532496.1:c.2230A>C
|
XP_011530798.1:p.Asn744His
|
|
NM_001320613.1:c.2830A>C
|
NP_001307542.1:p.Asn944His
|
|
NM_004036.4:c.2827A>C
|
NP_004027.2:p.Asn943His
|
|
XM_011532492.2:c.2953A>C
|
XP_011530794.1:p.Asn985His
|
|
XM_017003186.1:c.2893A>C
|
XP_016858675.1:p.Asn965His
|
|
XM_017003187.1:c.2884A>C
|
XP_016858676.1:p.Asn962His
|
|
XM_017003188.1:c.2950A>C
|
XP_016858677.1:p.Asn984His
|
|
XM_017003189.1:c.2812A>C
|
XP_016858678.1:p.Asn938His
|
|
XM_017003190.1:c.2689A>C
|
XP_016858679.1:p.Asn897His
|
|
XM_017003191.1:c.2317A>C
|
XP_016858680.1:p.Asn773His
|
|
XM_017003192.1:c.2107A>C
|
XP_016858681.1:p.Asn703His
|
|
XM_017003193.1:c.2104A>C
|
XP_016858682.1:p.Asn702His
|
|
NM_001320613.2:c.2830A>C
|
NP_001307542.1:p.Asn944His
|
|
NM_001377128.1:c.2893A>C
|
NP_001364057.1:p.Asn965His
|
|
NM_001377129.1:c.2689A>C
|
NP_001364058.1:p.Asn897His
|
|
NM_001377130.1:c.2332-635A>C
|
NP_001364059.1:n.2332-635A>C
|
|
NM_001377131.1:c.2104A>C
|
NP_001364060.1:p.Asn702His
|
|
NM_001377132.1:c.2827A>C
|
NP_001364061.1:p.Asn943His
|
|
NM_004036.5:c.2827A>C
MANE Select
|
NP_004027.2:p.Asn943His
|
|