ENST00000350026.11:c.4495A>T
|
ENSP00000055163.8:p.Arg1499Trp
|
|
ENST00000414678.8:c.4564A>T
|
ENSP00000412835.3:p.Arg1522Trp
|
|
ENST00000637015.2:c.4783A>T
|
ENSP00000489729.2:p.Arg1595Trp
|
|
ENST00000346085.10:c.4534A>T
|
ENSP00000344546.5:p.Arg1512Trp
|
|
ENST00000350026.10:c.4246A>T
|
ENSP00000055163.7:p.Arg1416Trp
|
|
ENST00000414678.7:c.2812A>T
|
ENSP00000412835.2:p.Arg938Trp
|
|
ENST00000635849.1:c.1975A>T
|
ENSP00000490948.1:p.Arg659Trp
|
|
ENST00000635957.1:c.1606A>T
|
ENSP00000490385.1:p.Arg536Trp
|
|
ENST00000636227.1:n.3117A>T
|
|
|
ENST00000636254.1:n.574A>T
|
|
|
ENST00000636930.2:c.4654A>T
MANE Select
|
ENSP00000490491.2:p.Arg1552Trp
|
|
ENST00000636940.1:n.2651A>T
|
|
|
ENST00000637015.1:c.2022A>T
|
|
|
ENST00000637568.1:c.1936A>T
|
|
|
ENST00000637741.1:n.1320A>T
|
|
|
ENST00000637810.1:c.1996A>T
|
ENSP00000489636.1:p.Arg666Trp
|
|
ENST00000637904.1:c.2155A>T
|
ENSP00000490550.1:p.Arg719Trp
|
|
ENST00000647938.1:c.4285A>T
|
ENSP00000498155.1:p.Arg1429Trp
|
|
ENST00000346085.9:c.4285A>T
|
ENSP00000344546.4:p.Arg1429Trp
|
|
ENST00000350026.9:c.4246A>T
|
ENSP00000055163.7:p.Arg1416Trp
|
|
ENST00000414678.6:c.2812A>T
|
ENSP00000412835.2:p.Arg938Trp
|
|
NM_017519.2:c.4246A>T
|
NP_059989.2:p.Arg1416Trp
|
|
NM_020732.3:c.4285A>T
|
NP_065783.3:p.Arg1429Trp
|
|
XM_005267069.3:c.4405A>T
|
XP_005267126.2:p.Arg1469Trp
|
|
XM_011535984.1:c.3484A>T
|
XP_011534286.1:p.Arg1162Trp
|
|
XM_011535985.1:c.3304A>T
|
XP_011534287.1:p.Arg1102Trp
|
|
XM_011535986.1:c.3064A>T
|
XP_011534288.1:p.Arg1022Trp
|
|
XM_011535987.1:c.2683A>T
|
XP_011534289.1:p.Arg895Trp
|
|
XM_011535988.1:c.1546A>T
|
XP_011534290.1:p.Arg516Trp
|
|
NM_001346813.1:c.4405A>T
|
NP_001333742.1:p.Arg1469Trp
|
|
NM_001363725.1:c.2155A>T
|
NP_001350654.1:p.Arg719Trp
|
|
XM_011535984.2:c.4615A>T
|
XP_011534286.2:p.Arg1539Trp
|
|
XM_011535988.3:c.1546A>T
|
XP_011534290.1:p.Arg516Trp
|
|
XM_017011103.2:c.4516A>T
|
XP_016866592.1:p.Arg1506Trp
|
|
XM_017011104.1:c.4486A>T
|
XP_016866593.1:p.Arg1496Trp
|
|
XM_017011105.2:c.4456A>T
|
XP_016866594.1:p.Arg1486Trp
|
|
XM_017011106.2:c.4327A>T
|
XP_016866595.1:p.Arg1443Trp
|
|
XM_017011107.2:c.4306A>T
|
XP_016866596.1:p.Arg1436Trp
|
|
XR_002956289.1:n.4601A>T
|
|
|
NM_001363725.2:c.2155A>T
|
NP_001350654.1:p.Arg719Trp
|
|
NM_001371656.1:c.4534A>T
|
NP_001358585.1:p.Arg1512Trp
|
|
NM_001374820.1:c.4534A>T
|
NP_001361749.1:p.Arg1512Trp
|
|
NM_001374828.1:c.4654A>T
MANE Select
|
NP_001361757.1:p.Arg1552Trp
|
|
NM_017519.3:c.4495A>T
|
NP_059989.3:p.Arg1499Trp
|
|