ENST00000262493.12:c.807C>T
MANE Select
|
ENSP00000262493.6:p.Leu269=
|
|
ENST00000562316.6:c.474C>T
|
ENSP00000457238.2:p.Leu158=
|
|
ENST00000564727.2:c.111C>T
|
ENSP00000454971.2:p.Leu37=
|
|
ENST00000568375.2:c.116-3399C>T
|
|
|
ENST00000638185.1:n.1022C>T
|
|
|
ENST00000638210.1:n.1107C>T
|
|
|
ENST00000638705.1:c.807C>T
|
ENSP00000491223.1:p.Leu269=
|
|
ENST00000638836.1:n.717C>T
|
|
|
ENST00000639055.1:n.1528C>T
|
|
|
ENST00000639251.1:n.708C>T
|
|
|
ENST00000639268.1:c.442C>T
|
|
|
ENST00000639341.1:c.332C>T
|
|
|
ENST00000639770.1:c.845C>T
|
ENSP00000491999.1:n.845C>T
|
|
ENST00000640390.1:n.737C>T
|
|
|
ENST00000640469.1:c.171C>T
|
ENSP00000491875.1:p.Leu57=
|
|
ENST00000640560.1:n.583C>T
|
|
|
ENST00000640893.1:c.*205C>T
|
ENSP00000492677.1:n.*205C>T
|
|
ENST00000262493.10:c.807C>T
|
ENSP00000262493.6:p.Leu269=
|
|
ENST00000564727.1:c.27C>T
|
ENSP00000454971.1:p.Leu9=
|
|
ENST00000568375.1:n.116-3399C>T
|
|
|
NM_020988.2:c.807C>T
|
NP_066268.1:p.Leu269=
|
|
XM_011523003.1:c.681C>T
|
XP_011521305.1:p.Leu227=
|
|
XM_011523003.3:c.681C>T
|
XP_011521305.1:p.Leu227=
|
|
NM_020988.3:c.807C>T
MANE Select
|
NP_066268.1:p.Leu269=
|
|