ENST00000262493.12:c.940T>A
MANE Select
|
ENSP00000262493.6:p.Ser314Thr
|
|
ENST00000562316.6:c.545-1175T>A
|
ENSP00000457238.2:n.545-1175T>A
|
|
ENST00000564727.2:c.244T>A
|
ENSP00000454971.2:p.Ser82Thr
|
|
ENST00000568375.2:c.178T>A
|
|
|
ENST00000638185.1:n.1155T>A
|
|
|
ENST00000638210.1:n.1240T>A
|
|
|
ENST00000638705.1:c.940T>A
|
ENSP00000491223.1:p.Ser314Thr
|
|
ENST00000638836.1:n.850T>A
|
|
|
ENST00000639055.1:n.1661T>A
|
|
|
ENST00000639251.1:n.841T>A
|
|
|
ENST00000639268.1:c.575T>A
|
|
|
ENST00000639341.1:c.465T>A
|
|
|
ENST00000639770.1:c.978T>A
|
ENSP00000491999.1:n.978T>A
|
|
ENST00000640390.1:n.870T>A
|
|
|
ENST00000640469.1:c.304T>A
|
ENSP00000491875.1:p.Ser102Thr
|
|
ENST00000640560.1:n.716T>A
|
|
|
ENST00000640893.1:c.*338T>A
|
ENSP00000492677.1:n.*338T>A
|
|
ENST00000262493.10:c.940T>A
|
ENSP00000262493.6:p.Ser314Thr
|
|
ENST00000564727.1:c.160T>A
|
ENSP00000454971.1:p.Ser54Thr
|
|
ENST00000568375.1:n.178T>A
|
|
|
NM_020988.2:c.940T>A
|
NP_066268.1:p.Ser314Thr
|
|
XM_011523003.1:c.814T>A
|
XP_011521305.1:p.Ser272Thr
|
|
XM_011523003.3:c.814T>A
|
XP_011521305.1:p.Ser272Thr
|
|
NM_020988.3:c.940T>A
MANE Select
|
NP_066268.1:p.Ser314Thr
|
|