ENST00000262493.12:c.1020C>A
MANE Select
|
ENSP00000262493.6:p.Thr340=
|
|
ENST00000562316.6:c.545-1095C>A
|
ENSP00000457238.2:n.545-1095C>A
|
|
ENST00000564727.2:c.303+21C>A
|
ENSP00000454971.2:n.303+21C>A
|
|
ENST00000568375.2:c.258C>A
|
|
|
ENST00000638210.1:n.1320C>A
|
|
|
ENST00000638705.1:c.1020C>A
|
ENSP00000491223.1:p.Thr340=
|
|
ENST00000638836.1:n.930C>A
|
|
|
ENST00000639251.1:n.921C>A
|
|
|
ENST00000639268.1:c.655C>A
|
|
|
ENST00000639341.1:c.545C>A
|
|
|
ENST00000639770.1:c.1058C>A
|
ENSP00000491999.1:n.1058C>A
|
|
ENST00000640390.1:n.950C>A
|
|
|
ENST00000640469.1:c.384C>A
|
ENSP00000491875.1:p.Thr128=
|
|
ENST00000640560.1:n.796C>A
|
|
|
ENST00000640893.1:c.*418C>A
|
ENSP00000492677.1:n.*418C>A
|
|
ENST00000262493.10:c.1020C>A
|
ENSP00000262493.6:p.Thr340=
|
|
ENST00000564727.1:c.240C>A
|
ENSP00000454971.1:p.Thr80=
|
|
ENST00000568375.1:n.258C>A
|
|
|
NM_020988.2:c.1020C>A
|
NP_066268.1:p.Thr340=
|
|
XM_011523003.1:c.894C>A
|
XP_011521305.1:p.Thr298=
|
|
XM_011523003.3:c.894C>A
|
XP_011521305.1:p.Thr298=
|
|
NM_020988.3:c.1020C>A
MANE Select
|
NP_066268.1:p.Thr340=
|
|