ENST00000262493.12:c.856A>G
MANE Select
|
ENSP00000262493.6:p.Ile286Val
|
|
ENST00000562316.6:c.523A>G
|
ENSP00000457238.2:p.Ile175Val
|
|
ENST00000564727.2:c.160A>G
|
ENSP00000454971.2:p.Ile54Val
|
|
ENST00000568375.2:c.116-3350A>G
|
|
|
ENST00000638185.1:n.1071A>G
|
|
|
ENST00000638210.1:n.1156A>G
|
|
|
ENST00000638705.1:c.856A>G
|
ENSP00000491223.1:p.Ile286Val
|
|
ENST00000638836.1:n.766A>G
|
|
|
ENST00000639055.1:n.1577A>G
|
|
|
ENST00000639251.1:n.757A>G
|
|
|
ENST00000639268.1:c.491A>G
|
|
|
ENST00000639341.1:c.381A>G
|
|
|
ENST00000639770.1:c.894A>G
|
ENSP00000491999.1:n.894A>G
|
|
ENST00000640390.1:n.786A>G
|
|
|
ENST00000640469.1:c.220A>G
|
ENSP00000491875.1:p.Ile74Val
|
|
ENST00000640560.1:n.632A>G
|
|
|
ENST00000640893.1:c.*254A>G
|
ENSP00000492677.1:n.*254A>G
|
|
ENST00000262493.10:c.856A>G
|
ENSP00000262493.6:p.Ile286Val
|
|
ENST00000564727.1:c.76A>G
|
ENSP00000454971.1:p.Ile26Val
|
|
ENST00000568375.1:n.116-3350A>G
|
|
|
NM_020988.2:c.856A>G
|
NP_066268.1:p.Ile286Val
|
|
XM_011523003.1:c.730A>G
|
XP_011521305.1:p.Ile244Val
|
|
XM_011523003.3:c.730A>G
|
XP_011521305.1:p.Ile244Val
|
|
NM_020988.3:c.856A>G
MANE Select
|
NP_066268.1:p.Ile286Val
|
|