ENST00000405392.6:c.2869A>T
|
ENSP00000384484.2:p.Ile957Phe
|
|
ENST00000679454.1:c.2866A>T
MANE Select
|
ENSP00000505261.1:p.Ile956Phe
|
|
ENST00000260600.9:c.2866A>T
|
ENSP00000260600.5:p.Ile956Phe
|
|
ENST00000405392.5:c.2869A>T
|
ENSP00000384484.2:p.Ile957Phe
|
|
ENST00000485887.1:n.138A>T
|
|
|
ENST00000606682.5:c.1807A>T
|
ENSP00000475652.1:p.Ile603Phe
|
|
NM_004036.3:c.2866A>T
|
NP_004027.2:p.Ile956Phe
|
|
XM_005264104.1:c.2869A>T
|
XP_005264161.1:p.Ile957Phe
|
|
XM_005264105.1:c.2866A>T
|
XP_005264162.1:p.Ile956Phe
|
|
XM_006711925.1:c.2935A>T
|
XP_006711988.1:p.Ile979Phe
|
|
XM_011532489.1:c.2992A>T
|
XP_011530791.1:p.Ile998Phe
|
|
XM_011532490.1:c.2989A>T
|
XP_011530792.1:p.Ile997Phe
|
|
XM_011532491.1:c.2926A>T
|
XP_011530793.1:p.Ile976Phe
|
|
XM_011532492.1:c.2992A>T
|
XP_011530794.1:p.Ile998Phe
|
|
XM_011532493.1:c.2854A>T
|
XP_011530795.1:p.Ile952Phe
|
|
XM_011532494.1:c.2794A>T
|
XP_011530796.1:p.Ile932Phe
|
|
XM_011532495.1:c.2326A>T
|
XP_011530797.1:p.Ile776Phe
|
|
XM_011532496.1:c.2269A>T
|
XP_011530798.1:p.Ile757Phe
|
|
NM_001320613.1:c.2869A>T
|
NP_001307542.1:p.Ile957Phe
|
|
NM_004036.4:c.2866A>T
|
NP_004027.2:p.Ile956Phe
|
|
XM_011532492.2:c.2992A>T
|
XP_011530794.1:p.Ile998Phe
|
|
XM_017003186.1:c.2932A>T
|
XP_016858675.1:p.Ile978Phe
|
|
XM_017003187.1:c.2923A>T
|
XP_016858676.1:p.Ile975Phe
|
|
XM_017003188.1:c.2989A>T
|
XP_016858677.1:p.Ile997Phe
|
|
XM_017003189.1:c.2851A>T
|
XP_016858678.1:p.Ile951Phe
|
|
XM_017003190.1:c.2728A>T
|
XP_016858679.1:p.Ile910Phe
|
|
XM_017003191.1:c.2356A>T
|
XP_016858680.1:p.Ile786Phe
|
|
XM_017003192.1:c.2146A>T
|
XP_016858681.1:p.Ile716Phe
|
|
XM_017003193.1:c.2143A>T
|
XP_016858682.1:p.Ile715Phe
|
|
NM_001320613.2:c.2869A>T
|
NP_001307542.1:p.Ile957Phe
|
|
NM_001377128.1:c.2932A>T
|
NP_001364057.1:p.Ile978Phe
|
|
NM_001377129.1:c.2728A>T
|
NP_001364058.1:p.Ile910Phe
|
|
NM_001377130.1:c.2332-596A>T
|
NP_001364059.1:n.2332-596A>T
|
|
NM_001377131.1:c.2143A>T
|
NP_001364060.1:p.Ile715Phe
|
|
NM_001377132.1:c.2866A>T
|
NP_001364061.1:p.Ile956Phe
|
|
NM_004036.5:c.2866A>T
MANE Select
|
NP_004027.2:p.Ile956Phe
|
|