ENST00000350026.11:c.3901A>T
|
ENSP00000055163.8:p.Ser1301Cys
|
|
ENST00000414678.8:c.3970A>T
|
ENSP00000412835.3:p.Ser1324Cys
|
|
ENST00000637015.2:c.4189A>T
|
ENSP00000489729.2:p.Ser1397Cys
|
|
ENST00000346085.10:c.3940A>T
|
ENSP00000344546.5:p.Ser1314Cys
|
|
ENST00000350026.10:c.3652A>T
|
ENSP00000055163.7:p.Ser1218Cys
|
|
ENST00000414678.7:c.2218A>T
|
ENSP00000412835.2:p.Ser740Cys
|
|
ENST00000635849.1:c.1381A>T
|
ENSP00000490948.1:p.Ser461Cys
|
|
ENST00000635957.1:c.1014-2A>T
|
ENSP00000490385.1:n.1014-2A>T
|
|
ENST00000636930.2:c.4060A>T
MANE Select
|
ENSP00000490491.2:p.Ser1354Cys
|
|
ENST00000636940.1:n.2057A>T
|
|
|
ENST00000637015.1:c.1428A>T
|
|
|
ENST00000637568.1:c.1342A>T
|
|
|
ENST00000637741.1:n.726A>T
|
|
|
ENST00000637810.1:c.1402A>T
|
ENSP00000489636.1:p.Ser468Cys
|
|
ENST00000637904.1:c.1561A>T
|
ENSP00000490550.1:p.Ser521Cys
|
|
ENST00000647938.1:c.3691A>T
|
ENSP00000498155.1:p.Ser1231Cys
|
|
ENST00000346085.9:c.3691A>T
|
ENSP00000344546.4:p.Ser1231Cys
|
|
ENST00000350026.9:c.3652A>T
|
ENSP00000055163.7:p.Ser1218Cys
|
|
ENST00000414678.6:c.2218A>T
|
ENSP00000412835.2:p.Ser740Cys
|
|
NM_017519.2:c.3652A>T
|
NP_059989.2:p.Ser1218Cys
|
|
NM_020732.3:c.3691A>T
|
NP_065783.3:p.Ser1231Cys
|
|
XM_005267069.3:c.3811A>T
|
XP_005267126.2:p.Ser1271Cys
|
|
XM_011535984.1:c.2890A>T
|
XP_011534286.1:p.Ser964Cys
|
|
XM_011535985.1:c.2710A>T
|
XP_011534287.1:p.Ser904Cys
|
|
XM_011535986.1:c.2470A>T
|
XP_011534288.1:p.Ser824Cys
|
|
XM_011535987.1:c.2089A>T
|
XP_011534289.1:p.Ser697Cys
|
|
XM_011535988.1:c.952A>T
|
XP_011534290.1:p.Ser318Cys
|
|
NM_001346813.1:c.3811A>T
|
NP_001333742.1:p.Ser1271Cys
|
|
NM_001363725.1:c.1561A>T
|
NP_001350654.1:p.Ser521Cys
|
|
XM_011535984.2:c.4021A>T
|
XP_011534286.2:p.Ser1341Cys
|
|
XM_011535988.3:c.952A>T
|
XP_011534290.1:p.Ser318Cys
|
|
XM_017011103.2:c.3922A>T
|
XP_016866592.1:p.Ser1308Cys
|
|
XM_017011104.1:c.3892A>T
|
XP_016866593.1:p.Ser1298Cys
|
|
XM_017011105.2:c.3862A>T
|
XP_016866594.1:p.Ser1288Cys
|
|
XM_017011106.2:c.3733A>T
|
XP_016866595.1:p.Ser1245Cys
|
|
XM_017011107.2:c.3712A>T
|
XP_016866596.1:p.Ser1238Cys
|
|
XR_002956289.1:n.4104A>T
|
|
|
NM_001363725.2:c.1561A>T
|
NP_001350654.1:p.Ser521Cys
|
|
NM_001371656.1:c.3940A>T
|
NP_001358585.1:p.Ser1314Cys
|
|
NM_001374820.1:c.3940A>T
|
NP_001361749.1:p.Ser1314Cys
|
|
NM_001374828.1:c.4060A>T
MANE Select
|
NP_001361757.1:p.Ser1354Cys
|
|
NM_017519.3:c.3901A>T
|
NP_059989.3:p.Ser1301Cys
|
|