ENST00000555134.2:n.988G>T
|
|
|
ENST00000556394.2:c.1604G>T
|
ENSP00000451967.2:p.Cys535Phe
|
|
ENST00000682247.1:c.2052G>T
|
ENSP00000507213.1:p.Leu684=
|
|
ENST00000682395.1:n.2527G>T
|
|
|
ENST00000682459.1:n.1766G>T
|
|
|
ENST00000682467.1:c.1922G>T
|
ENSP00000508062.1:p.Cys641Phe
|
|
ENST00000682795.1:c.2210G>T
|
ENSP00000507574.1:p.Cys737Phe
|
|
ENST00000682895.1:n.1779G>T
|
|
|
ENST00000682955.1:n.1637G>T
|
|
|
ENST00000683188.1:c.2324G>T
|
|
|
ENST00000683380.1:n.1727G>T
|
|
|
ENST00000683907.1:c.328G>T
|
ENSP00000507754.1:n.328G>T
|
|
ENST00000684259.1:n.3830G>T
|
|
|
ENST00000684538.1:n.1442G>T
|
|
|
ENST00000684549.1:n.1614G>T
|
|
|
ENST00000261534.9:c.2063G>T
MANE Select
|
ENSP00000261534.4:p.Cys688Phe
|
|
ENST00000261534.8:c.2063G>T
|
ENSP00000261534.4:p.Cys688Phe
|
|
ENST00000452340.7:n.3039G>T
|
|
|
ENST00000554767.5:n.2849G>T
|
|
|
ENST00000555710.1:c.424G>T
|
ENSP00000451730.1:n.424G>T
|
|
ENST00000556394.1:c.118G>T
|
|
|
ENST00000556446.1:n.364G>T
|
|
|
ENST00000602717.5:c.278G>T
|
ENSP00000487704.1:p.Cys93Phe
|
|
NM_013382.5:c.2063G>T , LRG_844t1:c.2063G>T
|
NP_037514.2:p.Cys688Phe
|
|
XM_011536675.1:c.2252G>T
|
XP_011534977.1:p.Cys751Phe
|
|
XM_011536676.1:c.1919G>T
|
XP_011534978.1:p.Cys640Phe
|
|
XM_011536677.1:c.1793G>T
|
XP_011534979.1:p.Cys598Phe
|
|
XM_011536679.1:c.1346G>T
|
XP_011534981.1:p.Cys449Phe
|
|
XR_943416.1:n.2316G>T
|
|
|
XM_011536675.2:c.2252G>T
|
XP_011534977.1:p.Cys751Phe
|
|
XM_011536676.2:c.1919G>T
|
XP_011534978.1:p.Cys640Phe
|
|
XM_011536677.3:c.1793G>T
|
XP_011534979.1:p.Cys598Phe
|
|
XR_001750279.1:n.2349G>T
|
|
|
XR_001750282.1:n.3002G>T
|
|
|
XR_943416.3:n.2314G>T
|
|
|
NM_013382.6:c.2063G>T
|
NP_037514.2:p.Cys688Phe
|
|
NM_013382.7:c.2063G>T
MANE Select
|
NP_037514.2:p.Cys688Phe
|
|