ENST00000262493.12:c.749T>G
MANE Select
|
ENSP00000262493.6:p.Leu250Arg
|
|
ENST00000562316.6:c.416T>G
|
ENSP00000457238.2:p.Leu139Arg
|
|
ENST00000564727.2:c.53T>G
|
ENSP00000454971.2:p.Leu18Arg
|
|
ENST00000568375.2:c.116-3457T>G
|
|
|
ENST00000638185.1:n.964T>G
|
|
|
ENST00000638210.1:n.1049T>G
|
|
|
ENST00000638705.1:c.749T>G
|
ENSP00000491223.1:p.Leu250Arg
|
|
ENST00000638836.1:n.659T>G
|
|
|
ENST00000639055.1:n.1470T>G
|
|
|
ENST00000639251.1:n.650T>G
|
|
|
ENST00000639268.1:c.384T>G
|
|
|
ENST00000639341.1:c.274T>G
|
|
|
ENST00000639770.1:c.787T>G
|
ENSP00000491999.1:n.787T>G
|
|
ENST00000640390.1:n.679T>G
|
|
|
ENST00000640469.1:c.113T>G
|
ENSP00000491875.1:p.Leu38Arg
|
|
ENST00000640560.1:n.525T>G
|
|
|
ENST00000640893.1:c.*147T>G
|
ENSP00000492677.1:n.*147T>G
|
|
ENST00000262493.10:c.749T>G
|
ENSP00000262493.6:p.Leu250Arg
|
|
ENST00000568375.1:n.116-3457T>G
|
|
|
NM_020988.2:c.749T>G
|
NP_066268.1:p.Leu250Arg
|
|
XM_011523003.1:c.623T>G
|
XP_011521305.1:p.Leu208Arg
|
|
XM_011523003.3:c.623T>G
|
XP_011521305.1:p.Leu208Arg
|
|
NM_020988.3:c.749T>G
MANE Select
|
NP_066268.1:p.Leu250Arg
|
|