ENST00000262493.12:c.780C>T
MANE Select
|
ENSP00000262493.6:p.Phe260=
|
|
ENST00000562316.6:c.447C>T
|
ENSP00000457238.2:p.Phe149=
|
|
ENST00000564727.2:c.84C>T
|
ENSP00000454971.2:p.Phe28=
|
|
ENST00000568375.2:c.116-3426C>T
|
|
|
ENST00000638185.1:n.995C>T
|
|
|
ENST00000638210.1:n.1080C>T
|
|
|
ENST00000638705.1:c.780C>T
|
ENSP00000491223.1:p.Phe260=
|
|
ENST00000638836.1:n.690C>T
|
|
|
ENST00000639055.1:n.1501C>T
|
|
|
ENST00000639251.1:n.681C>T
|
|
|
ENST00000639268.1:c.415C>T
|
|
|
ENST00000639341.1:c.305C>T
|
|
|
ENST00000639770.1:c.818C>T
|
ENSP00000491999.1:n.818C>T
|
|
ENST00000640390.1:n.710C>T
|
|
|
ENST00000640469.1:c.144C>T
|
ENSP00000491875.1:p.Phe48=
|
|
ENST00000640560.1:n.556C>T
|
|
|
ENST00000640893.1:c.*178C>T
|
ENSP00000492677.1:n.*178C>T
|
|
ENST00000262493.10:c.780C>T
|
ENSP00000262493.6:p.Phe260=
|
|
ENST00000568375.1:n.116-3426C>T
|
|
|
NM_020988.2:c.780C>T
|
NP_066268.1:p.Phe260=
|
|
XM_011523003.1:c.654C>T
|
XP_011521305.1:p.Phe218=
|
|
XM_011523003.3:c.654C>T
|
XP_011521305.1:p.Phe218=
|
|
NM_020988.3:c.780C>T
MANE Select
|
NP_066268.1:p.Phe260=
|
|