ENST00000262493.12:c.792C>T
MANE Select
|
ENSP00000262493.6:p.Ser264=
|
|
ENST00000562316.6:c.459C>T
|
ENSP00000457238.2:p.Ser153=
|
|
ENST00000564727.2:c.96C>T
|
ENSP00000454971.2:p.Ser32=
|
|
ENST00000568375.2:c.116-3414C>T
|
|
|
ENST00000638185.1:n.1007C>T
|
|
|
ENST00000638210.1:n.1092C>T
|
|
|
ENST00000638705.1:c.792C>T
|
ENSP00000491223.1:p.Ser264=
|
|
ENST00000638836.1:n.702C>T
|
|
|
ENST00000639055.1:n.1513C>T
|
|
|
ENST00000639251.1:n.693C>T
|
|
|
ENST00000639268.1:c.427C>T
|
|
|
ENST00000639341.1:c.317C>T
|
|
|
ENST00000639770.1:c.830C>T
|
ENSP00000491999.1:n.830C>T
|
|
ENST00000640390.1:n.722C>T
|
|
|
ENST00000640469.1:c.156C>T
|
ENSP00000491875.1:p.Ser52=
|
|
ENST00000640560.1:n.568C>T
|
|
|
ENST00000640893.1:c.*190C>T
|
ENSP00000492677.1:n.*190C>T
|
|
ENST00000262493.10:c.792C>T
|
ENSP00000262493.6:p.Ser264=
|
|
ENST00000564727.1:c.12C>T
|
ENSP00000454971.1:p.Ser4=
|
|
ENST00000568375.1:n.116-3414C>T
|
|
|
NM_020988.2:c.792C>T
|
NP_066268.1:p.Ser264=
|
|
XM_011523003.1:c.666C>T
|
XP_011521305.1:p.Ser222=
|
|
XM_011523003.3:c.666C>T
|
XP_011521305.1:p.Ser222=
|
|
NM_020988.3:c.792C>T
MANE Select
|
NP_066268.1:p.Ser264=
|
|