ENST00000258168.7:c.702C>T
MANE Select
|
ENSP00000258168.2:p.Ser234=
|
|
ENST00000258168.6:c.702C>T
|
ENSP00000258168.2:p.Ser234=
|
|
ENST00000563804.5:c.*326C>T
|
ENSP00000457910.1:n.*326C>T
|
|
NM_017429.2:c.702C>T
|
NP_059125.2:p.Ser234=
|
|
XM_011523109.1:c.702C>T
|
XP_011521411.1:p.Ser234=
|
|
XM_011523110.1:c.153C>T
|
XP_011521412.1:p.Ser51=
|
|
XM_011523109.2:c.702C>T
|
XP_011521411.1:p.Ser234=
|
|
XM_017023286.2:c.702C>T
|
XP_016878775.1:p.Ser234=
|
|
XM_017023287.2:c.702C>T
|
XP_016878776.1:p.Ser234=
|
|
XM_017023288.2:c.702C>T
|
XP_016878777.1:p.Ser234=
|
|
XM_017023289.1:c.-24-52C>T
|
XP_016878778.1:n.-24-52C>T
|
|
XR_002957813.1:n.1081-52C>T
|
|
|
NM_017429.3:c.702C>T
MANE Select
|
NP_059125.2:p.Ser234=
|
|