ENST00000350026.11:c.3457A>T
|
ENSP00000055163.8:p.Arg1153Ter
|
|
ENST00000414678.8:c.3526A>T
|
ENSP00000412835.3:p.Arg1176Ter
|
|
ENST00000637015.2:c.3745A>T
|
ENSP00000489729.2:p.Arg1249Ter
|
|
ENST00000319584.11:c.1630A>T
|
ENSP00000313006.7:p.Arg544Ter
|
|
ENST00000346085.10:c.3496A>T
|
ENSP00000344546.5:p.Arg1166Ter
|
|
ENST00000350026.10:c.3208A>T
|
ENSP00000055163.7:p.Arg1070Ter
|
|
ENST00000414678.7:c.1774A>T
|
ENSP00000412835.2:p.Arg592Ter
|
|
ENST00000635849.1:c.937A>T
|
ENSP00000490948.1:p.Arg313Ter
|
|
ENST00000635957.1:c.571A>T
|
ENSP00000490385.1:p.Arg191Ter
|
|
ENST00000636930.2:c.3616A>T
MANE Select
|
ENSP00000490491.2:p.Arg1206Ter
|
|
ENST00000636940.1:n.1613A>T
|
|
|
ENST00000637015.1:c.984A>T
|
|
|
ENST00000637568.1:c.898A>T
|
|
|
ENST00000637741.1:n.282A>T
|
|
|
ENST00000637810.1:c.958A>T
|
ENSP00000489636.1:p.Arg320Ter
|
|
ENST00000637904.1:c.1117A>T
|
ENSP00000490550.1:p.Arg373Ter
|
|
ENST00000647938.1:c.3247A>T
|
ENSP00000498155.1:p.Arg1083Ter
|
|
ENST00000319584.10:c.1633A>T
|
ENSP00000313006.6:p.Arg545Ter
|
|
ENST00000346085.9:c.3247A>T
|
ENSP00000344546.4:p.Arg1083Ter
|
|
ENST00000350026.9:c.3208A>T
|
ENSP00000055163.7:p.Arg1070Ter
|
|
ENST00000400790.3:c.409A>T
|
ENSP00000383596.3:p.Arg137Ter
|
|
ENST00000414678.6:c.1774A>T
|
ENSP00000412835.2:p.Arg592Ter
|
|
ENST00000478761.3:c.818A>T
|
|
|
NM_017519.2:c.3208A>T
|
NP_059989.2:p.Arg1070Ter
|
|
NM_020732.3:c.3247A>T
|
NP_065783.3:p.Arg1083Ter
|
|
XM_005267069.3:c.3367A>T
|
XP_005267126.2:p.Arg1123Ter
|
|
XM_011535984.1:c.2446A>T
|
XP_011534286.1:p.Arg816Ter
|
|
XM_011535985.1:c.2266A>T
|
XP_011534287.1:p.Arg756Ter
|
|
XM_011535986.1:c.2026A>T
|
XP_011534288.1:p.Arg676Ter
|
|
XM_011535987.1:c.1645A>T
|
XP_011534289.1:p.Arg549Ter
|
|
XM_011535988.1:c.508A>T
|
XP_011534290.1:p.Arg170Ter
|
|
NM_001346813.1:c.3367A>T
|
NP_001333742.1:p.Arg1123Ter
|
|
NM_001363725.1:c.1117A>T
|
NP_001350654.1:p.Arg373Ter
|
|
XM_011535984.2:c.3577A>T
|
XP_011534286.2:p.Arg1193Ter
|
|
XM_011535988.3:c.508A>T
|
XP_011534290.1:p.Arg170Ter
|
|
XM_017011103.2:c.3478A>T
|
XP_016866592.1:p.Arg1160Ter
|
|
XM_017011104.1:c.3448A>T
|
XP_016866593.1:p.Arg1150Ter
|
|
XM_017011105.2:c.3418A>T
|
XP_016866594.1:p.Arg1140Ter
|
|
XM_017011106.2:c.3289A>T
|
XP_016866595.1:p.Arg1097Ter
|
|
XM_017011107.2:c.3268A>T
|
XP_016866596.1:p.Arg1090Ter
|
|
XR_002956289.1:n.3660A>T
|
|
|
NM_001363725.2:c.1117A>T
|
NP_001350654.1:p.Arg373Ter
|
|
NM_001371656.1:c.3496A>T
|
NP_001358585.1:p.Arg1166Ter
|
|
NM_001374820.1:c.3496A>T
|
NP_001361749.1:p.Arg1166Ter
|
|
NM_001374828.1:c.3616A>T
MANE Select
|
NP_001361757.1:p.Arg1206Ter
|
|
NM_017519.3:c.3457A>T
|
NP_059989.3:p.Arg1153Ter
|
|