ENST00000262493.12:c.747G>T
MANE Select
|
ENSP00000262493.6:p.Met249Ile
|
|
ENST00000562316.6:c.414G>T
|
ENSP00000457238.2:p.Met138Ile
|
|
ENST00000564727.2:c.51G>T
|
ENSP00000454971.2:p.Met17Ile
|
|
ENST00000568375.2:c.116-3459G>T
|
|
|
ENST00000638185.1:n.962G>T
|
|
|
ENST00000638210.1:n.1047G>T
|
|
|
ENST00000638705.1:c.747G>T
|
ENSP00000491223.1:p.Met249Ile
|
|
ENST00000638836.1:n.657G>T
|
|
|
ENST00000639055.1:n.1468G>T
|
|
|
ENST00000639251.1:n.648G>T
|
|
|
ENST00000639268.1:c.382G>T
|
|
|
ENST00000639341.1:c.272G>T
|
|
|
ENST00000639770.1:c.785G>T
|
ENSP00000491999.1:n.785G>T
|
|
ENST00000640390.1:n.677G>T
|
|
|
ENST00000640469.1:c.111G>T
|
ENSP00000491875.1:p.Met37Ile
|
|
ENST00000640560.1:n.523G>T
|
|
|
ENST00000640893.1:c.*145G>T
|
ENSP00000492677.1:n.*145G>T
|
|
ENST00000262493.10:c.747G>T
|
ENSP00000262493.6:p.Met249Ile
|
|
ENST00000568375.1:n.116-3459G>T
|
|
|
NM_020988.2:c.747G>T
|
NP_066268.1:p.Met249Ile
|
|
XM_011523003.1:c.621G>T
|
XP_011521305.1:p.Met207Ile
|
|
XM_011523003.3:c.621G>T
|
XP_011521305.1:p.Met207Ile
|
|
NM_020988.3:c.747G>T
MANE Select
|
NP_066268.1:p.Met249Ile
|
|