|
NM_145038.5:c.528C>T
MANE Select
|
NP_659475.2:p.Ser176=
|
|
ENST00000288710.7:c.528C>T
MANE Select
|
ENSP00000288710.2:p.Ser176=
|
|
NM_145038.3:c.528C>T
|
NP_659475.2:p.Ser176=
|
|
NM_145038.4:c.528C>T
|
NP_659475.2:p.Ser176=
|
|
ENST00000288710.6:c.528C>T
|
ENSP00000288710.2:p.Ser176=
|
|
ENST00000421869.5:c.356+3042C>T
|
ENSP00000414375.1:n.356+3042C>T
|
|
ENST00000487307.5:n.247+3042C>T
|
|
|
ENST00000497651.1:n.418C>T
|
|
|
ENST00000649059.1:c.514C>T
|
|
|
XM_005264637.3:c.-79+3042C>T
|
XP_005264694.1:n.-79+3042C>T
|
|
XM_005264638.3:c.-341+3042C>T
|
XP_005264695.1:n.-341+3042C>T
|
|
XM_017005271.1:c.-353C>T
|
XP_016860760.1:n.-353C>T
|
|
XM_024453218.1:c.-341+3042C>T
|
XP_024308986.1:n.-341+3042C>T
|