ENST00000555134.2:n.817-209G>T
|
|
|
ENST00000556394.2:c.1433-209G>T
|
ENSP00000451967.2:n.1433-209G>T
|
|
ENST00000682128.1:c.193-209G>T
|
ENSP00000506976.1:n.193-209G>T
|
|
ENST00000682247.1:c.1892-220G>T
|
ENSP00000507213.1:n.1892-220G>T
|
|
ENST00000682395.1:n.2356-209G>T
|
|
|
ENST00000682459.1:n.1595-209G>T
|
|
|
ENST00000682467.1:c.1892-570G>T
|
ENSP00000508062.1:n.1892-570G>T
|
|
ENST00000682615.1:n.246-209G>T
|
|
|
ENST00000682795.1:c.2039-209G>T
|
ENSP00000507574.1:n.2039-209G>T
|
|
ENST00000682895.1:n.1608-209G>T
|
|
|
ENST00000682955.1:n.1466-209G>T
|
|
|
ENST00000683095.1:c.298-209G>T
|
ENSP00000508040.1:n.298-209G>T
|
|
ENST00000683188.1:c.2153-209G>T
|
|
|
ENST00000683380.1:n.1556-209G>T
|
|
|
ENST00000683828.1:c.1601-209G>T
|
|
|
ENST00000683907.1:c.157-209G>T
|
ENSP00000507754.1:n.157-209G>T
|
|
ENST00000684172.1:c.268-209G>T
|
ENSP00000508391.1:n.268-209G>T
|
|
ENST00000684259.1:n.3450G>T
|
|
|
ENST00000684538.1:n.1062G>T
|
|
|
ENST00000684549.1:n.1443-209G>T
|
|
|
ENST00000261534.9:c.1892-209G>T
MANE Select
|
ENSP00000261534.4:n.1892-209G>T
|
|
ENST00000261534.8:c.1892-209G>T
|
ENSP00000261534.4:n.1892-209G>T
|
|
ENST00000452340.7:n.2659G>T
|
|
|
ENST00000554767.5:n.2678-209G>T
|
|
|
ENST00000555134.1:n.817-209G>T
|
|
|
ENST00000555710.1:c.161-117G>T
|
ENSP00000451730.1:n.161-117G>T
|
|
ENST00000556171.1:c.484-209G>T
|
|
|
ENST00000556394.1:c.88-570G>T
|
|
|
ENST00000602717.5:c.107-209G>T
|
ENSP00000487704.1:n.107-209G>T
|
|
NM_013382.5:c.1892-209G>T , LRG_844t1:c.1892-209G>T
|
NP_037514.2:n.1892-209G>T
|
|
XM_011536675.1:c.2081-209G>T
|
XP_011534977.1:n.2081-209G>T
|
|
XM_011536676.1:c.1748-209G>T
|
XP_011534978.1:n.1748-209G>T
|
|
XM_011536677.1:c.1622-209G>T
|
XP_011534979.1:n.1622-209G>T
|
|
XM_011536678.1:c.*420G>T
|
XP_011534980.1:n.*420G>T
|
|
XM_011536679.1:c.1175-209G>T
|
XP_011534981.1:n.1175-209G>T
|
|
XR_943416.1:n.2145-209G>T
|
|
|
XM_011536675.2:c.2081-209G>T
|
XP_011534977.1:n.2081-209G>T
|
|
XM_011536676.2:c.1748-209G>T
|
XP_011534978.1:n.1748-209G>T
|
|
XM_011536677.3:c.1622-209G>T
|
XP_011534979.1:n.1622-209G>T
|
|
XR_001750279.1:n.2178-209G>T
|
|
|
XR_001750282.1:n.2831-209G>T
|
|
|
XR_943416.3:n.2143-209G>T
|
|
|
NM_013382.6:c.1892-209G>T
|
NP_037514.2:n.1892-209G>T
|
|
NM_013382.7:c.1892-209G>T
MANE Select
|
NP_037514.2:n.1892-209G>T
|
|