ENST00000371757.7:c.314T>C
MANE Select
|
ENSP00000360822.2:p.Phe105Ser
|
|
ENST00000637018.1:n.119T>C
|
|
|
ENST00000638123.1:n.49T>C
|
|
|
ENST00000674572.1:c.155T>C
|
ENSP00000501742.1:p.Phe52Ser
|
|
ENST00000675090.1:c.62T>C
|
ENSP00000501833.1:p.Phe21Ser
|
|
ENST00000675399.1:c.62T>C
|
ENSP00000501932.1:p.Phe21Ser
|
|
ENST00000676421.1:c.62T>C
|
ENSP00000502322.1:p.Phe21Ser
|
|
ENST00000263604.5:c.215T>C
|
ENSP00000263604.4:p.Phe72Ser
|
|
ENST00000371757.6:c.314T>C
|
ENSP00000360822.2:p.Phe105Ser
|
|
ENST00000460750.5:c.314T>C
|
ENSP00000418777.1:p.Phe105Ser
|
|
ENST00000473941.5:c.155T>C
|
ENSP00000420764.1:p.Phe52Ser
|
|
ENST00000486577.6:c.197T>C
|
ENSP00000417578.3:p.Phe66Ser
|
|
ENST00000487664.5:c.314T>C
|
ENSP00000417851.2:p.Phe105Ser
|
|
ENST00000488444.6:c.257T>C
|
ENSP00000419007.3:p.Phe86Ser
|
|
ENST00000490355.6:c.257T>C
|
ENSP00000418003.3:p.Phe86Ser
|
|
ENST00000491806.6:c.257T>C
|
ENSP00000419086.3:p.Phe86Ser
|
|
ENST00000628528.2:c.170T>C
|
ENSP00000486374.1:p.Phe57Ser
|
|
ENST00000630792.2:c.155T>C
|
ENSP00000486486.1:p.Phe52Ser
|
|
ENST00000631073.2:c.257T>C
|
ENSP00000486130.1:p.Phe86Ser
|
|
NM_001272003.1:c.170T>C
|
NP_001258932.1:p.Phe57Ser
|
|
NM_020822.2:c.314T>C
|
NP_065873.2:p.Phe105Ser
|
|
XM_011518877.1:c.449T>C
|
XP_011517179.1:p.Phe150Ser
|
|
XM_011518878.1:c.449T>C
|
XP_011517180.1:p.Phe150Ser
|
|
XM_011518879.1:c.449T>C
|
XP_011517181.1:p.Phe150Ser
|
|
XM_011518880.1:c.215T>C
|
XP_011517182.1:p.Phe72Ser
|
|
XM_011518877.3:c.449T>C
|
XP_011517179.1:p.Phe150Ser
|
|
XM_011518878.3:c.449T>C
|
XP_011517180.1:p.Phe150Ser
|
|
XM_011518879.3:c.449T>C
|
XP_011517181.1:p.Phe150Ser
|
|
XM_017014931.1:c.339T>C
|
XP_016870420.1:p.Leu113=
|
|
XM_017014932.1:c.62T>C
|
XP_016870421.1:p.Phe21Ser
|
|
XM_017014933.1:c.-106T>C
|
XP_016870422.1:n.-106T>C
|
|
XM_024447617.1:c.-206T>C
|
XP_024303385.1:n.-206T>C
|
|
XM_024447618.1:c.-206T>C
|
XP_024303386.1:n.-206T>C
|
|
NM_020822.3:c.314T>C
MANE Select
|
NP_065873.2:p.Phe105Ser
|
|
NM_001272003.2:c.170T>C
|
NP_001258932.1:p.Phe57Ser
|
|