ENST00000405392.6:c.2798T>C
|
ENSP00000384484.2:p.Phe933Ser
|
|
ENST00000679454.1:c.2795T>C
MANE Select
|
ENSP00000505261.1:p.Phe932Ser
|
|
ENST00000260600.9:c.2795T>C
|
ENSP00000260600.5:p.Phe932Ser
|
|
ENST00000405392.5:c.2798T>C
|
ENSP00000384484.2:p.Phe933Ser
|
|
ENST00000485887.1:n.67T>C
|
|
|
ENST00000606682.5:c.1736T>C
|
ENSP00000475652.1:p.Phe579Ser
|
|
NM_004036.3:c.2795T>C
|
NP_004027.2:p.Phe932Ser
|
|
XM_005264104.1:c.2798T>C
|
XP_005264161.1:p.Phe933Ser
|
|
XM_005264105.1:c.2795T>C
|
XP_005264162.1:p.Phe932Ser
|
|
XM_006711925.1:c.2864T>C
|
XP_006711988.1:p.Phe955Ser
|
|
XM_011532489.1:c.2921T>C
|
XP_011530791.1:p.Phe974Ser
|
|
XM_011532490.1:c.2918T>C
|
XP_011530792.1:p.Phe973Ser
|
|
XM_011532491.1:c.2855T>C
|
XP_011530793.1:p.Phe952Ser
|
|
XM_011532492.1:c.2921T>C
|
XP_011530794.1:p.Phe974Ser
|
|
XM_011532493.1:c.2783T>C
|
XP_011530795.1:p.Phe928Ser
|
|
XM_011532494.1:c.2723T>C
|
XP_011530796.1:p.Phe908Ser
|
|
XM_011532495.1:c.2255T>C
|
XP_011530797.1:p.Phe752Ser
|
|
XM_011532496.1:c.2198T>C
|
XP_011530798.1:p.Phe733Ser
|
|
NM_001320613.1:c.2798T>C
|
NP_001307542.1:p.Phe933Ser
|
|
NM_004036.4:c.2795T>C
|
NP_004027.2:p.Phe932Ser
|
|
XM_011532492.2:c.2921T>C
|
XP_011530794.1:p.Phe974Ser
|
|
XM_017003186.1:c.2861T>C
|
XP_016858675.1:p.Phe954Ser
|
|
XM_017003187.1:c.2852T>C
|
XP_016858676.1:p.Phe951Ser
|
|
XM_017003188.1:c.2918T>C
|
XP_016858677.1:p.Phe973Ser
|
|
XM_017003189.1:c.2780T>C
|
XP_016858678.1:p.Phe927Ser
|
|
XM_017003190.1:c.2657T>C
|
XP_016858679.1:p.Phe886Ser
|
|
XM_017003191.1:c.2285T>C
|
XP_016858680.1:p.Phe762Ser
|
|
XM_017003192.1:c.2075T>C
|
XP_016858681.1:p.Phe692Ser
|
|
XM_017003193.1:c.2072T>C
|
XP_016858682.1:p.Phe691Ser
|
|
NM_001320613.2:c.2798T>C
|
NP_001307542.1:p.Phe933Ser
|
|
NM_001377128.1:c.2861T>C
|
NP_001364057.1:p.Phe954Ser
|
|
NM_001377129.1:c.2657T>C
|
NP_001364058.1:p.Phe886Ser
|
|
NM_001377130.1:c.2332-667T>C
|
NP_001364059.1:n.2332-667T>C
|
|
NM_001377131.1:c.2072T>C
|
NP_001364060.1:p.Phe691Ser
|
|
NM_001377132.1:c.2795T>C
|
NP_001364061.1:p.Phe932Ser
|
|
NM_004036.5:c.2795T>C
MANE Select
|
NP_004027.2:p.Phe932Ser
|
|