ENST00000262493.12:c.833A>T
MANE Select
|
ENSP00000262493.6:p.Lys278Met
|
|
ENST00000562316.6:c.500A>T
|
ENSP00000457238.2:p.Lys167Met
|
|
ENST00000564727.2:c.137A>T
|
ENSP00000454971.2:p.Lys46Met
|
|
ENST00000568375.2:c.116-3373A>T
|
|
|
ENST00000638185.1:n.1048A>T
|
|
|
ENST00000638210.1:n.1133A>T
|
|
|
ENST00000638705.1:c.833A>T
|
ENSP00000491223.1:p.Lys278Met
|
|
ENST00000638836.1:n.743A>T
|
|
|
ENST00000639055.1:n.1554A>T
|
|
|
ENST00000639251.1:n.734A>T
|
|
|
ENST00000639268.1:c.468A>T
|
|
|
ENST00000639341.1:c.358A>T
|
|
|
ENST00000639770.1:c.871A>T
|
ENSP00000491999.1:n.871A>T
|
|
ENST00000640390.1:n.763A>T
|
|
|
ENST00000640469.1:c.197A>T
|
ENSP00000491875.1:p.Lys66Met
|
|
ENST00000640560.1:n.609A>T
|
|
|
ENST00000640893.1:c.*231A>T
|
ENSP00000492677.1:n.*231A>T
|
|
ENST00000262493.10:c.833A>T
|
ENSP00000262493.6:p.Lys278Met
|
|
ENST00000564727.1:c.53A>T
|
ENSP00000454971.1:p.Lys18Met
|
|
ENST00000568375.1:n.116-3373A>T
|
|
|
NM_020988.2:c.833A>T
|
NP_066268.1:p.Lys278Met
|
|
XM_011523003.1:c.707A>T
|
XP_011521305.1:p.Lys236Met
|
|
XM_011523003.3:c.707A>T
|
XP_011521305.1:p.Lys236Met
|
|
NM_020988.3:c.833A>T
MANE Select
|
NP_066268.1:p.Lys278Met
|
|