ENST00000555134.2:n.979T>G
|
|
|
ENST00000556394.2:c.1595T>G
|
ENSP00000451967.2:p.Leu532Arg
|
|
ENST00000682247.1:c.2043T>G
|
ENSP00000507213.1:p.Pro681=
|
|
ENST00000682395.1:n.2518T>G
|
|
|
ENST00000682459.1:n.1757T>G
|
|
|
ENST00000682467.1:c.1913T>G
|
ENSP00000508062.1:p.Leu638Arg
|
|
ENST00000682795.1:c.2201T>G
|
ENSP00000507574.1:p.Leu734Arg
|
|
ENST00000682895.1:n.1770T>G
|
|
|
ENST00000682955.1:n.1628T>G
|
|
|
ENST00000683188.1:c.2315T>G
|
|
|
ENST00000683380.1:n.1718T>G
|
|
|
ENST00000683907.1:c.319T>G
|
ENSP00000507754.1:n.319T>G
|
|
ENST00000684259.1:n.3821T>G
|
|
|
ENST00000684538.1:n.1433T>G
|
|
|
ENST00000684549.1:n.1605T>G
|
|
|
ENST00000261534.9:c.2054T>G
MANE Select
|
ENSP00000261534.4:p.Leu685Arg
|
|
ENST00000261534.8:c.2054T>G
|
ENSP00000261534.4:p.Leu685Arg
|
|
ENST00000452340.7:n.3030T>G
|
|
|
ENST00000554767.5:n.2840T>G
|
|
|
ENST00000555710.1:c.415T>G
|
ENSP00000451730.1:n.415T>G
|
|
ENST00000556394.1:c.109T>G
|
|
|
ENST00000556446.1:n.355T>G
|
|
|
ENST00000602717.5:c.269T>G
|
ENSP00000487704.1:p.Leu90Arg
|
|
NM_013382.5:c.2054T>G , LRG_844t1:c.2054T>G
|
NP_037514.2:p.Leu685Arg
|
|
XM_011536675.1:c.2243T>G
|
XP_011534977.1:p.Leu748Arg
|
|
XM_011536676.1:c.1910T>G
|
XP_011534978.1:p.Leu637Arg
|
|
XM_011536677.1:c.1784T>G
|
XP_011534979.1:p.Leu595Arg
|
|
XM_011536679.1:c.1337T>G
|
XP_011534981.1:p.Leu446Arg
|
|
XR_943416.1:n.2307T>G
|
|
|
XM_011536675.2:c.2243T>G
|
XP_011534977.1:p.Leu748Arg
|
|
XM_011536676.2:c.1910T>G
|
XP_011534978.1:p.Leu637Arg
|
|
XM_011536677.3:c.1784T>G
|
XP_011534979.1:p.Leu595Arg
|
|
XR_001750279.1:n.2340T>G
|
|
|
XR_001750282.1:n.2993T>G
|
|
|
XR_943416.3:n.2305T>G
|
|
|
NM_013382.6:c.2054T>G
|
NP_037514.2:p.Leu685Arg
|
|
NM_013382.7:c.2054T>G
MANE Select
|
NP_037514.2:p.Leu685Arg
|
|