ENST00000405392.6:c.2777T>C
|
ENSP00000384484.2:p.Met926Thr
|
|
ENST00000679454.1:c.2774T>C
MANE Select
|
ENSP00000505261.1:p.Met925Thr
|
|
ENST00000260600.9:c.2774T>C
|
ENSP00000260600.5:p.Met925Thr
|
|
ENST00000405392.5:c.2777T>C
|
ENSP00000384484.2:p.Met926Thr
|
|
ENST00000485887.1:n.46T>C
|
|
|
ENST00000606682.5:c.1715T>C
|
ENSP00000475652.1:p.Met572Thr
|
|
NM_004036.3:c.2774T>C
|
NP_004027.2:p.Met925Thr
|
|
XM_005264104.1:c.2777T>C
|
XP_005264161.1:p.Met926Thr
|
|
XM_005264105.1:c.2774T>C
|
XP_005264162.1:p.Met925Thr
|
|
XM_006711925.1:c.2843T>C
|
XP_006711988.1:p.Met948Thr
|
|
XM_011532489.1:c.2900T>C
|
XP_011530791.1:p.Met967Thr
|
|
XM_011532490.1:c.2897T>C
|
XP_011530792.1:p.Met966Thr
|
|
XM_011532491.1:c.2834T>C
|
XP_011530793.1:p.Met945Thr
|
|
XM_011532492.1:c.2900T>C
|
XP_011530794.1:p.Met967Thr
|
|
XM_011532493.1:c.2762T>C
|
XP_011530795.1:p.Met921Thr
|
|
XM_011532494.1:c.2702T>C
|
XP_011530796.1:p.Met901Thr
|
|
XM_011532495.1:c.2234T>C
|
XP_011530797.1:p.Met745Thr
|
|
XM_011532496.1:c.2177T>C
|
XP_011530798.1:p.Met726Thr
|
|
NM_001320613.1:c.2777T>C
|
NP_001307542.1:p.Met926Thr
|
|
NM_004036.4:c.2774T>C
|
NP_004027.2:p.Met925Thr
|
|
XM_011532492.2:c.2900T>C
|
XP_011530794.1:p.Met967Thr
|
|
XM_017003186.1:c.2840T>C
|
XP_016858675.1:p.Met947Thr
|
|
XM_017003187.1:c.2831T>C
|
XP_016858676.1:p.Met944Thr
|
|
XM_017003188.1:c.2897T>C
|
XP_016858677.1:p.Met966Thr
|
|
XM_017003189.1:c.2759T>C
|
XP_016858678.1:p.Met920Thr
|
|
XM_017003190.1:c.2636T>C
|
XP_016858679.1:p.Met879Thr
|
|
XM_017003191.1:c.2264T>C
|
XP_016858680.1:p.Met755Thr
|
|
XM_017003192.1:c.2054T>C
|
XP_016858681.1:p.Met685Thr
|
|
XM_017003193.1:c.2051T>C
|
XP_016858682.1:p.Met684Thr
|
|
NM_001320613.2:c.2777T>C
|
NP_001307542.1:p.Met926Thr
|
|
NM_001377128.1:c.2840T>C
|
NP_001364057.1:p.Met947Thr
|
|
NM_001377129.1:c.2636T>C
|
NP_001364058.1:p.Met879Thr
|
|
NM_001377130.1:c.2332-688T>C
|
NP_001364059.1:n.2332-688T>C
|
|
NM_001377131.1:c.2051T>C
|
NP_001364060.1:p.Met684Thr
|
|
NM_001377132.1:c.2774T>C
|
NP_001364061.1:p.Met925Thr
|
|
NM_004036.5:c.2774T>C
MANE Select
|
NP_004027.2:p.Met925Thr
|
|