ENST00000350026.11:c.3981C>T
|
ENSP00000055163.8:p.Asn1327=
|
|
ENST00000414678.8:c.4050C>T
|
ENSP00000412835.3:p.Asn1350=
|
|
ENST00000637015.2:c.4269C>T
|
ENSP00000489729.2:p.Asn1423=
|
|
ENST00000346085.10:c.4020C>T
|
ENSP00000344546.5:p.Asn1340=
|
|
ENST00000350026.10:c.3732C>T
|
ENSP00000055163.7:p.Asn1244=
|
|
ENST00000414678.7:c.2298C>T
|
ENSP00000412835.2:p.Asn766=
|
|
ENST00000635849.1:c.1461C>T
|
ENSP00000490948.1:p.Asn487=
|
|
ENST00000635957.1:c.1092C>T
|
ENSP00000490385.1:p.Asn364=
|
|
ENST00000636930.2:c.4140C>T
MANE Select
|
ENSP00000490491.2:p.Asn1380=
|
|
ENST00000636940.1:n.2137C>T
|
|
|
ENST00000637015.1:c.1508C>T
|
|
|
ENST00000637568.1:c.1422C>T
|
|
|
ENST00000637741.1:n.806C>T
|
|
|
ENST00000637810.1:c.1482C>T
|
ENSP00000489636.1:p.Asn494=
|
|
ENST00000637904.1:c.1641C>T
|
ENSP00000490550.1:p.Asn547=
|
|
ENST00000647938.1:c.3771C>T
|
ENSP00000498155.1:p.Asn1257=
|
|
ENST00000346085.9:c.3771C>T
|
ENSP00000344546.4:p.Asn1257=
|
|
ENST00000350026.9:c.3732C>T
|
ENSP00000055163.7:p.Asn1244=
|
|
ENST00000414678.6:c.2298C>T
|
ENSP00000412835.2:p.Asn766=
|
|
NM_017519.2:c.3732C>T
|
NP_059989.2:p.Asn1244=
|
|
NM_020732.3:c.3771C>T
|
NP_065783.3:p.Asn1257=
|
|
XM_005267069.3:c.3891C>T
|
XP_005267126.2:p.Asn1297=
|
|
XM_011535984.1:c.2970C>T
|
XP_011534286.1:p.Asn990=
|
|
XM_011535985.1:c.2790C>T
|
XP_011534287.1:p.Asn930=
|
|
XM_011535986.1:c.2550C>T
|
XP_011534288.1:p.Asn850=
|
|
XM_011535987.1:c.2169C>T
|
XP_011534289.1:p.Asn723=
|
|
XM_011535988.1:c.1032C>T
|
XP_011534290.1:p.Asn344=
|
|
NM_001346813.1:c.3891C>T
|
NP_001333742.1:p.Asn1297=
|
|
NM_001363725.1:c.1641C>T
|
NP_001350654.1:p.Asn547=
|
|
XM_011535984.2:c.4101C>T
|
XP_011534286.2:p.Asn1367=
|
|
XM_011535988.3:c.1032C>T
|
XP_011534290.1:p.Asn344=
|
|
XM_017011103.2:c.4002C>T
|
XP_016866592.1:p.Asn1334=
|
|
XM_017011104.1:c.3972C>T
|
XP_016866593.1:p.Asn1324=
|
|
XM_017011105.2:c.3942C>T
|
XP_016866594.1:p.Asn1314=
|
|
XM_017011106.2:c.3813C>T
|
XP_016866595.1:p.Asn1271=
|
|
XM_017011107.2:c.3792C>T
|
XP_016866596.1:p.Asn1264=
|
|
XR_002956289.1:n.4184C>T
|
|
|
NM_001363725.2:c.1641C>T
|
NP_001350654.1:p.Asn547=
|
|
NM_001371656.1:c.4020C>T
|
NP_001358585.1:p.Asn1340=
|
|
NM_001374820.1:c.4020C>T
|
NP_001361749.1:p.Asn1340=
|
|
NM_001374828.1:c.4140C>T
MANE Select
|
NP_001361757.1:p.Asn1380=
|
|
NM_017519.3:c.3981C>T
|
NP_059989.3:p.Asn1327=
|
|