|
ENST00000703936.1:c.2664G>T
|
ENSP00000515567.1:p.Lys888Asn
|
|
|
ENST00000703937.1:c.*1725G>T
|
ENSP00000515568.1:n.*1725G>T
|
|
|
ENST00000326739.9:c.624G>T
MANE Select
|
ENSP00000321584.4:p.Lys208Asn
|
|
|
ENST00000429182.6:c.624G>T
|
ENSP00000393525.2:p.Lys208Asn
|
|
|
ENST00000442157.2:c.549G>T
|
ENSP00000403502.2:p.Lys183Asn
|
|
|
ENST00000462980.2:n.1139G>T
|
|
|
|
ENST00000472328.2:n.690G>T
|
|
|
|
ENST00000491610.2:n.584G>T
|
|
|
|
ENST00000676607.1:n.920G>T
|
|
|
|
ENST00000676627.1:n.1354G>T
|
|
|
|
ENST00000676708.1:n.1904G>T
|
|
|
|
ENST00000676864.1:n.1773G>T
|
|
|
|
ENST00000677010.1:c.660G>T
|
ENSP00000503089.1:p.Lys220Asn
|
|
|
ENST00000677108.1:n.2530G>T
|
|
|
|
ENST00000677168.1:n.1096G>T
|
|
|
|
ENST00000677185.1:n.1187G>T
|
|
|
|
ENST00000677205.1:n.1408G>T
|
|
|
|
ENST00000677344.1:n.1898G>T
|
|
|
|
ENST00000677480.1:c.*301G>T
|
ENSP00000504378.1:n.*301G>T
|
|
|
ENST00000677519.1:n.1334G>T
|
|
|
|
ENST00000677593.1:n.1180G>T
|
|
|
|
ENST00000677740.1:n.2129G>T
|
|
|
|
ENST00000677991.1:n.1797G>T
|
|
|
|
ENST00000678001.1:n.1117G>T
|
|
|
|
ENST00000678085.1:n.1180G>T
|
|
|
|
ENST00000678177.1:n.2473G>T
|
|
|
|
ENST00000678603.1:n.1702G>T
|
|
|
|
ENST00000678724.1:c.549G>T
|
ENSP00000503874.1:p.Lys183Asn
|
|
|
ENST00000678920.1:n.782G>T
|
|
|
|
ENST00000679019.1:n.1394G>T
|
|
|
|
ENST00000679117.1:c.*439G>T
|
ENSP00000503240.1:n.*439G>T
|
|
|
ENST00000679339.1:n.1465G>T
|
|
|
|
ENST00000326739.8:c.624G>T
|
ENSP00000321584.4:p.Lys208Asn
|
|
|
ENST00000429182.5:c.418G>T
|
|
|
|
ENST00000442157.1:c.549G>T
|
ENSP00000403502.1:p.Lys183Asn
|
|
|
ENST00000462980.1:n.526G>T
|
|
|
|
ENST00000491610.1:n.584G>T
|
|
|
|
NM_000884.2:c.624G>T
|
NP_000875.2:p.Lys208Asn
|
|
|
XM_006713128.2:c.834G>T
|
XP_006713191.1:p.Lys278Asn
|
|
|
XM_006713128.3:c.834G>T
|
XP_006713191.1:p.Lys278Asn
|
|
|
XM_017006349.1:c.759G>T
|
XP_016861838.1:p.Lys253Asn
|
|
|
XM_017006350.1:c.759G>T
|
XP_016861839.1:p.Lys253Asn
|
|
|
NM_000884.3:c.624G>T
MANE Select
|
NP_000875.2:p.Lys208Asn
|
|
