ENST00000298910.12:c.3492T>C
MANE Select
|
ENSP00000298910.7:p.Phe1164=
|
|
ENST00000679360.1:c.*2401T>C
|
ENSP00000505368.1:n.*2401T>C
|
|
ENST00000680790.1:c.3237T>C
|
ENSP00000505335.1:p.Phe1079=
|
|
ENST00000298910.11:c.3492T>C
|
ENSP00000298910.7:p.Phe1164=
|
|
ENST00000343742.6:c.3492T>C
|
ENSP00000341930.2:p.Phe1164=
|
|
ENST00000430804.5:c.536T>C
|
|
|
ENST00000479187.5:n.173T>C
|
|
|
NM_198578.3:c.3492T>C
|
NP_940980.3:p.Phe1164=
|
|
XM_005268629.2:c.3492T>C
|
XP_005268686.1:p.Phe1164=
|
|
XM_011537877.1:c.3492T>C
|
XP_011536179.1:p.Phe1164=
|
|
XM_011537878.1:c.3492T>C
|
XP_011536180.1:p.Phe1164=
|
|
XM_011537879.1:c.2289T>C
|
XP_011536181.1:p.Phe763=
|
|
XM_011537880.1:c.3492T>C
|
XP_011536182.1:p.Phe1164=
|
|
XM_011537881.1:c.3492T>C
|
XP_011536183.1:p.Phe1164=
|
|
XM_011537882.1:c.3492T>C
|
XP_011536184.1:p.Phe1164=
|
|
XM_005268629.4:c.3492T>C
|
XP_005268686.1:p.Phe1164=
|
|
XM_011537877.3:c.3492T>C
|
XP_011536179.1:p.Phe1164=
|
|
XM_011537881.3:c.3492T>C
|
XP_011536183.1:p.Phe1164=
|
|
XM_011537882.3:c.3492T>C
|
XP_011536184.1:p.Phe1164=
|
|
XM_017018786.2:c.3492T>C
|
XP_016874275.1:p.Phe1164=
|
|
XM_017018787.1:c.408T>C
|
XP_016874276.1:p.Phe136=
|
|
XM_017018789.2:c.3492T>C
|
XP_016874278.1:p.Phe1164=
|
|
XM_024448833.1:c.2289T>C
|
XP_024304601.1:p.Phe763=
|
|
XR_001748574.2:n.3734T>C
|
|
|
NM_198578.4:c.3492T>C
MANE Select
|
NP_940980.4:p.Phe1164=
|
|