ENST00000273064.11:c.261T>G
MANE Select
|
ENSP00000273064.6:p.Ser87=
|
|
ENST00000273064.10:c.261T>G
|
ENSP00000273064.6:p.Ser87=
|
|
ENST00000295701.9:c.261T>G
|
ENSP00000295701.5:p.Ser87=
|
|
ENST00000432877.5:c.*153T>G
|
ENSP00000392394.1:n.*153T>G
|
|
ENST00000542068.5:c.261T>G
|
ENSP00000443687.1:p.Ser87=
|
|
ENST00000627282.2:c.261T>G
|
ENSP00000486540.1:p.Ser87=
|
|
NM_001271634.1:c.261T>G
|
NP_001258563.1:p.Ser87=
|
|
NM_001271635.1:c.261T>G
|
NP_001258564.1:p.Ser87=
|
|
NM_005444.2:c.261T>G
|
NP_005435.1:p.Ser87=
|
|
NR_073390.1:n.636T>G
|
|
|
XM_011512138.1:c.102T>G
|
XP_011510440.1:p.Ser34=
|
|
XM_011512138.3:c.102T>G
|
XP_011510440.1:p.Ser34=
|
|
XM_017005248.1:c.99T>G
|
XP_016860737.1:p.Ser33=
|
|
XM_017005249.2:c.102T>G
|
XP_016860738.1:p.Ser34=
|
|
NM_001271634.2:c.261T>G
|
NP_001258563.1:p.Ser87=
|
|
NM_005444.3:c.261T>G
MANE Select
|
NP_005435.1:p.Ser87=
|
|
NR_073390.2:n.377T>G
|
|
|
NM_001271635.2:c.261T>G
|
NP_001258564.1:p.Ser87=
|
|