ENST00000350026.11:c.3966C>G
|
ENSP00000055163.8:p.Asn1322Lys
|
|
ENST00000414678.8:c.4035C>G
|
ENSP00000412835.3:p.Asn1345Lys
|
|
ENST00000637015.2:c.4254C>G
|
ENSP00000489729.2:p.Asn1418Lys
|
|
ENST00000346085.10:c.4005C>G
|
ENSP00000344546.5:p.Asn1335Lys
|
|
ENST00000350026.10:c.3717C>G
|
ENSP00000055163.7:p.Asn1239Lys
|
|
ENST00000414678.7:c.2283C>G
|
ENSP00000412835.2:p.Asn761Lys
|
|
ENST00000635849.1:c.1446C>G
|
ENSP00000490948.1:p.Asn482Lys
|
|
ENST00000635957.1:c.1077C>G
|
ENSP00000490385.1:p.Asn359Lys
|
|
ENST00000636930.2:c.4125C>G
MANE Select
|
ENSP00000490491.2:p.Asn1375Lys
|
|
ENST00000636940.1:n.2122C>G
|
|
|
ENST00000637015.1:c.1493C>G
|
|
|
ENST00000637568.1:c.1407C>G
|
|
|
ENST00000637741.1:n.791C>G
|
|
|
ENST00000637810.1:c.1467C>G
|
ENSP00000489636.1:p.Asn489Lys
|
|
ENST00000637904.1:c.1626C>G
|
ENSP00000490550.1:p.Asn542Lys
|
|
ENST00000647938.1:c.3756C>G
|
ENSP00000498155.1:p.Asn1252Lys
|
|
ENST00000346085.9:c.3756C>G
|
ENSP00000344546.4:p.Asn1252Lys
|
|
ENST00000350026.9:c.3717C>G
|
ENSP00000055163.7:p.Asn1239Lys
|
|
ENST00000414678.6:c.2283C>G
|
ENSP00000412835.2:p.Asn761Lys
|
|
NM_017519.2:c.3717C>G
|
NP_059989.2:p.Asn1239Lys
|
|
NM_020732.3:c.3756C>G
|
NP_065783.3:p.Asn1252Lys
|
|
XM_005267069.3:c.3876C>G
|
XP_005267126.2:p.Asn1292Lys
|
|
XM_011535984.1:c.2955C>G
|
XP_011534286.1:p.Asn985Lys
|
|
XM_011535985.1:c.2775C>G
|
XP_011534287.1:p.Asn925Lys
|
|
XM_011535986.1:c.2535C>G
|
XP_011534288.1:p.Asn845Lys
|
|
XM_011535987.1:c.2154C>G
|
XP_011534289.1:p.Asn718Lys
|
|
XM_011535988.1:c.1017C>G
|
XP_011534290.1:p.Asn339Lys
|
|
NM_001346813.1:c.3876C>G
|
NP_001333742.1:p.Asn1292Lys
|
|
NM_001363725.1:c.1626C>G
|
NP_001350654.1:p.Asn542Lys
|
|
XM_011535984.2:c.4086C>G
|
XP_011534286.2:p.Asn1362Lys
|
|
XM_011535988.3:c.1017C>G
|
XP_011534290.1:p.Asn339Lys
|
|
XM_017011103.2:c.3987C>G
|
XP_016866592.1:p.Asn1329Lys
|
|
XM_017011104.1:c.3957C>G
|
XP_016866593.1:p.Asn1319Lys
|
|
XM_017011105.2:c.3927C>G
|
XP_016866594.1:p.Asn1309Lys
|
|
XM_017011106.2:c.3798C>G
|
XP_016866595.1:p.Asn1266Lys
|
|
XM_017011107.2:c.3777C>G
|
XP_016866596.1:p.Asn1259Lys
|
|
XR_002956289.1:n.4169C>G
|
|
|
NM_001363725.2:c.1626C>G
|
NP_001350654.1:p.Asn542Lys
|
|
NM_001371656.1:c.4005C>G
|
NP_001358585.1:p.Asn1335Lys
|
|
NM_001374820.1:c.4005C>G
|
NP_001361749.1:p.Asn1335Lys
|
|
NM_001374828.1:c.4125C>G
MANE Select
|
NP_001361757.1:p.Asn1375Lys
|
|
NM_017519.3:c.3966C>G
|
NP_059989.3:p.Asn1322Lys
|
|