ENST00000555134.2:n.921T>G
|
|
|
ENST00000556394.2:c.1537T>G
|
ENSP00000451967.2:p.Tyr513Asp
|
|
ENST00000682128.1:c.297T>G
|
ENSP00000506976.1:n.297T>G
|
|
ENST00000682247.1:c.1985T>G
|
ENSP00000507213.1:p.Leu662Arg
|
|
ENST00000682395.1:n.2460T>G
|
|
|
ENST00000682459.1:n.1699T>G
|
|
|
ENST00000682467.1:c.1892-257T>G
|
ENSP00000508062.1:n.1892-257T>G
|
|
ENST00000682615.1:n.350T>G
|
|
|
ENST00000682795.1:c.2143T>G
|
ENSP00000507574.1:p.Tyr715Asp
|
|
ENST00000682895.1:n.1712T>G
|
|
|
ENST00000682955.1:n.1570T>G
|
|
|
ENST00000683095.1:c.402T>G
|
ENSP00000508040.1:n.402T>G
|
|
ENST00000683188.1:c.2257T>G
|
|
|
ENST00000683380.1:n.1660T>G
|
|
|
ENST00000683907.1:c.261T>G
|
ENSP00000507754.1:n.261T>G
|
|
ENST00000684172.1:c.372T>G
|
ENSP00000508391.1:n.372T>G
|
|
ENST00000684259.1:n.3763T>G
|
|
|
ENST00000684538.1:n.1375T>G
|
|
|
ENST00000684549.1:n.1547T>G
|
|
|
ENST00000261534.9:c.1996T>G
MANE Select
|
ENSP00000261534.4:p.Tyr666Asp
|
|
ENST00000261534.8:c.1996T>G
|
ENSP00000261534.4:p.Tyr666Asp
|
|
ENST00000452340.7:n.2972T>G
|
|
|
ENST00000554767.5:n.2782T>G
|
|
|
ENST00000555710.1:c.357T>G
|
ENSP00000451730.1:n.357T>G
|
|
ENST00000556394.1:c.88-257T>G
|
|
|
ENST00000556446.1:n.297T>G
|
|
|
ENST00000602717.5:c.211T>G
|
ENSP00000487704.1:p.Tyr71Asp
|
|
NM_013382.5:c.1996T>G , LRG_844t1:c.1996T>G
|
NP_037514.2:p.Tyr666Asp
|
|
XM_011536675.1:c.2185T>G
|
XP_011534977.1:p.Tyr729Asp
|
|
XM_011536676.1:c.1852T>G
|
XP_011534978.1:p.Tyr618Asp
|
|
XM_011536677.1:c.1726T>G
|
XP_011534979.1:p.Tyr576Asp
|
|
XM_011536679.1:c.1279T>G
|
XP_011534981.1:p.Tyr427Asp
|
|
XR_943416.1:n.2249T>G
|
|
|
XM_011536675.2:c.2185T>G
|
XP_011534977.1:p.Tyr729Asp
|
|
XM_011536676.2:c.1852T>G
|
XP_011534978.1:p.Tyr618Asp
|
|
XM_011536677.3:c.1726T>G
|
XP_011534979.1:p.Tyr576Asp
|
|
XR_001750279.1:n.2282T>G
|
|
|
XR_001750282.1:n.2935T>G
|
|
|
XR_943416.3:n.2247T>G
|
|
|
NM_013382.6:c.1996T>G
|
NP_037514.2:p.Tyr666Asp
|
|
NM_013382.7:c.1996T>G
MANE Select
|
NP_037514.2:p.Tyr666Asp
|
|