ENST00000262493.12:c.805C>T
MANE Select
|
ENSP00000262493.6:p.Leu269Phe
|
|
ENST00000562316.6:c.472C>T
|
ENSP00000457238.2:p.Leu158Phe
|
|
ENST00000564727.2:c.109C>T
|
ENSP00000454971.2:p.Leu37Phe
|
|
ENST00000568375.2:c.116-3401C>T
|
|
|
ENST00000638185.1:n.1020C>T
|
|
|
ENST00000638210.1:n.1105C>T
|
|
|
ENST00000638705.1:c.805C>T
|
ENSP00000491223.1:p.Leu269Phe
|
|
ENST00000638836.1:n.715C>T
|
|
|
ENST00000639055.1:n.1526C>T
|
|
|
ENST00000639251.1:n.706C>T
|
|
|
ENST00000639268.1:c.440C>T
|
|
|
ENST00000639341.1:c.330C>T
|
|
|
ENST00000639770.1:c.843C>T
|
ENSP00000491999.1:n.843C>T
|
|
ENST00000640390.1:n.735C>T
|
|
|
ENST00000640469.1:c.169C>T
|
ENSP00000491875.1:p.Leu57Phe
|
|
ENST00000640560.1:n.581C>T
|
|
|
ENST00000640893.1:c.*203C>T
|
ENSP00000492677.1:n.*203C>T
|
|
ENST00000262493.10:c.805C>T
|
ENSP00000262493.6:p.Leu269Phe
|
|
ENST00000564727.1:c.25C>T
|
ENSP00000454971.1:p.Leu9Phe
|
|
ENST00000568375.1:n.116-3401C>T
|
|
|
NM_020988.2:c.805C>T
|
NP_066268.1:p.Leu269Phe
|
|
XM_011523003.1:c.679C>T
|
XP_011521305.1:p.Leu227Phe
|
|
XM_011523003.3:c.679C>T
|
XP_011521305.1:p.Leu227Phe
|
|
NM_020988.3:c.805C>T
MANE Select
|
NP_066268.1:p.Leu269Phe
|
|