ENST00000405392.6:c.2801C>A
|
ENSP00000384484.2:p.Ala934Asp
|
|
ENST00000679454.1:c.2798C>A
MANE Select
|
ENSP00000505261.1:p.Ala933Asp
|
|
ENST00000260600.9:c.2798C>A
|
ENSP00000260600.5:p.Ala933Asp
|
|
ENST00000405392.5:c.2801C>A
|
ENSP00000384484.2:p.Ala934Asp
|
|
ENST00000485887.1:n.70C>A
|
|
|
ENST00000606682.5:c.1739C>A
|
ENSP00000475652.1:p.Ala580Asp
|
|
NM_004036.3:c.2798C>A
|
NP_004027.2:p.Ala933Asp
|
|
XM_005264104.1:c.2801C>A
|
XP_005264161.1:p.Ala934Asp
|
|
XM_005264105.1:c.2798C>A
|
XP_005264162.1:p.Ala933Asp
|
|
XM_006711925.1:c.2867C>A
|
XP_006711988.1:p.Ala956Asp
|
|
XM_011532489.1:c.2924C>A
|
XP_011530791.1:p.Ala975Asp
|
|
XM_011532490.1:c.2921C>A
|
XP_011530792.1:p.Ala974Asp
|
|
XM_011532491.1:c.2858C>A
|
XP_011530793.1:p.Ala953Asp
|
|
XM_011532492.1:c.2924C>A
|
XP_011530794.1:p.Ala975Asp
|
|
XM_011532493.1:c.2786C>A
|
XP_011530795.1:p.Ala929Asp
|
|
XM_011532494.1:c.2726C>A
|
XP_011530796.1:p.Ala909Asp
|
|
XM_011532495.1:c.2258C>A
|
XP_011530797.1:p.Ala753Asp
|
|
XM_011532496.1:c.2201C>A
|
XP_011530798.1:p.Ala734Asp
|
|
NM_001320613.1:c.2801C>A
|
NP_001307542.1:p.Ala934Asp
|
|
NM_004036.4:c.2798C>A
|
NP_004027.2:p.Ala933Asp
|
|
XM_011532492.2:c.2924C>A
|
XP_011530794.1:p.Ala975Asp
|
|
XM_017003186.1:c.2864C>A
|
XP_016858675.1:p.Ala955Asp
|
|
XM_017003187.1:c.2855C>A
|
XP_016858676.1:p.Ala952Asp
|
|
XM_017003188.1:c.2921C>A
|
XP_016858677.1:p.Ala974Asp
|
|
XM_017003189.1:c.2783C>A
|
XP_016858678.1:p.Ala928Asp
|
|
XM_017003190.1:c.2660C>A
|
XP_016858679.1:p.Ala887Asp
|
|
XM_017003191.1:c.2288C>A
|
XP_016858680.1:p.Ala763Asp
|
|
XM_017003192.1:c.2078C>A
|
XP_016858681.1:p.Ala693Asp
|
|
XM_017003193.1:c.2075C>A
|
XP_016858682.1:p.Ala692Asp
|
|
NM_001320613.2:c.2801C>A
|
NP_001307542.1:p.Ala934Asp
|
|
NM_001377128.1:c.2864C>A
|
NP_001364057.1:p.Ala955Asp
|
|
NM_001377129.1:c.2660C>A
|
NP_001364058.1:p.Ala887Asp
|
|
NM_001377130.1:c.2332-664C>A
|
NP_001364059.1:n.2332-664C>A
|
|
NM_001377131.1:c.2075C>A
|
NP_001364060.1:p.Ala692Asp
|
|
NM_001377132.1:c.2798C>A
|
NP_001364061.1:p.Ala933Asp
|
|
NM_004036.5:c.2798C>A
MANE Select
|
NP_004027.2:p.Ala933Asp
|
|