ENST00000262493.12:c.820C>G
MANE Select
|
ENSP00000262493.6:p.Leu274Val
|
|
ENST00000562316.6:c.487C>G
|
ENSP00000457238.2:p.Leu163Val
|
|
ENST00000564727.2:c.124C>G
|
ENSP00000454971.2:p.Leu42Val
|
|
ENST00000568375.2:c.116-3386C>G
|
|
|
ENST00000638185.1:n.1035C>G
|
|
|
ENST00000638210.1:n.1120C>G
|
|
|
ENST00000638705.1:c.820C>G
|
ENSP00000491223.1:p.Leu274Val
|
|
ENST00000638836.1:n.730C>G
|
|
|
ENST00000639055.1:n.1541C>G
|
|
|
ENST00000639251.1:n.721C>G
|
|
|
ENST00000639268.1:c.455C>G
|
|
|
ENST00000639341.1:c.345C>G
|
|
|
ENST00000639770.1:c.858C>G
|
ENSP00000491999.1:n.858C>G
|
|
ENST00000640390.1:n.750C>G
|
|
|
ENST00000640469.1:c.184C>G
|
ENSP00000491875.1:p.Leu62Val
|
|
ENST00000640560.1:n.596C>G
|
|
|
ENST00000640893.1:c.*218C>G
|
ENSP00000492677.1:n.*218C>G
|
|
ENST00000262493.10:c.820C>G
|
ENSP00000262493.6:p.Leu274Val
|
|
ENST00000564727.1:c.40C>G
|
ENSP00000454971.1:p.Leu14Val
|
|
ENST00000568375.1:n.116-3386C>G
|
|
|
NM_020988.2:c.820C>G
|
NP_066268.1:p.Leu274Val
|
|
XM_011523003.1:c.694C>G
|
XP_011521305.1:p.Leu232Val
|
|
XM_011523003.3:c.694C>G
|
XP_011521305.1:p.Leu232Val
|
|
NM_020988.3:c.820C>G
MANE Select
|
NP_066268.1:p.Leu274Val
|
|