ENST00000350026.11:c.3901A>C
|
ENSP00000055163.8:p.Ser1301Arg
|
|
ENST00000414678.8:c.3970A>C
|
ENSP00000412835.3:p.Ser1324Arg
|
|
ENST00000637015.2:c.4189A>C
|
ENSP00000489729.2:p.Ser1397Arg
|
|
ENST00000346085.10:c.3940A>C
|
ENSP00000344546.5:p.Ser1314Arg
|
|
ENST00000350026.10:c.3652A>C
|
ENSP00000055163.7:p.Ser1218Arg
|
|
ENST00000414678.7:c.2218A>C
|
ENSP00000412835.2:p.Ser740Arg
|
|
ENST00000635849.1:c.1381A>C
|
ENSP00000490948.1:p.Ser461Arg
|
|
ENST00000635957.1:c.1014-2A>C
|
ENSP00000490385.1:n.1014-2A>C
|
|
ENST00000636930.2:c.4060A>C
MANE Select
|
ENSP00000490491.2:p.Ser1354Arg
|
|
ENST00000636940.1:n.2057A>C
|
|
|
ENST00000637015.1:c.1428A>C
|
|
|
ENST00000637568.1:c.1342A>C
|
|
|
ENST00000637741.1:n.726A>C
|
|
|
ENST00000637810.1:c.1402A>C
|
ENSP00000489636.1:p.Ser468Arg
|
|
ENST00000637904.1:c.1561A>C
|
ENSP00000490550.1:p.Ser521Arg
|
|
ENST00000647938.1:c.3691A>C
|
ENSP00000498155.1:p.Ser1231Arg
|
|
ENST00000346085.9:c.3691A>C
|
ENSP00000344546.4:p.Ser1231Arg
|
|
ENST00000350026.9:c.3652A>C
|
ENSP00000055163.7:p.Ser1218Arg
|
|
ENST00000414678.6:c.2218A>C
|
ENSP00000412835.2:p.Ser740Arg
|
|
NM_017519.2:c.3652A>C
|
NP_059989.2:p.Ser1218Arg
|
|
NM_020732.3:c.3691A>C
|
NP_065783.3:p.Ser1231Arg
|
|
XM_005267069.3:c.3811A>C
|
XP_005267126.2:p.Ser1271Arg
|
|
XM_011535984.1:c.2890A>C
|
XP_011534286.1:p.Ser964Arg
|
|
XM_011535985.1:c.2710A>C
|
XP_011534287.1:p.Ser904Arg
|
|
XM_011535986.1:c.2470A>C
|
XP_011534288.1:p.Ser824Arg
|
|
XM_011535987.1:c.2089A>C
|
XP_011534289.1:p.Ser697Arg
|
|
XM_011535988.1:c.952A>C
|
XP_011534290.1:p.Ser318Arg
|
|
NM_001346813.1:c.3811A>C
|
NP_001333742.1:p.Ser1271Arg
|
|
NM_001363725.1:c.1561A>C
|
NP_001350654.1:p.Ser521Arg
|
|
XM_011535984.2:c.4021A>C
|
XP_011534286.2:p.Ser1341Arg
|
|
XM_011535988.3:c.952A>C
|
XP_011534290.1:p.Ser318Arg
|
|
XM_017011103.2:c.3922A>C
|
XP_016866592.1:p.Ser1308Arg
|
|
XM_017011104.1:c.3892A>C
|
XP_016866593.1:p.Ser1298Arg
|
|
XM_017011105.2:c.3862A>C
|
XP_016866594.1:p.Ser1288Arg
|
|
XM_017011106.2:c.3733A>C
|
XP_016866595.1:p.Ser1245Arg
|
|
XM_017011107.2:c.3712A>C
|
XP_016866596.1:p.Ser1238Arg
|
|
XR_002956289.1:n.4104A>C
|
|
|
NM_001363725.2:c.1561A>C
|
NP_001350654.1:p.Ser521Arg
|
|
NM_001371656.1:c.3940A>C
|
NP_001358585.1:p.Ser1314Arg
|
|
NM_001374820.1:c.3940A>C
|
NP_001361749.1:p.Ser1314Arg
|
|
NM_001374828.1:c.4060A>C
MANE Select
|
NP_001361757.1:p.Ser1354Arg
|
|
NM_017519.3:c.3901A>C
|
NP_059989.3:p.Ser1301Arg
|
|