ENST00000377443.7:c.357G>T
MANE Select
|
ENSP00000366662.2:p.Ser119=
|
|
ENST00000377436.6:c.357G>T
|
ENSP00000366654.3:p.Ser119=
|
|
ENST00000377442.3:c.177G>T
|
ENSP00000366661.2:p.Ser59=
|
|
ENST00000377443.6:c.357G>T
|
ENSP00000366662.2:p.Ser119=
|
|
ENST00000476083.1:n.99-1676G>T
|
|
|
ENST00000549778.5:c.261G>T
|
ENSP00000447108.1:p.Ser87=
|
|
NM_001215.3:c.357G>T
|
NP_001206.2:p.Ser119=
|
|
NM_001270500.1:c.357G>T
|
NP_001257429.1:p.Ser119=
|
|
NM_001270501.1:c.177G>T
|
NP_001257430.1:p.Ser59=
|
|
NM_001270502.1:c.25-1676G>T
|
NP_001257431.1:n.25-1676G>T
|
|
XM_011542083.1:c.369G>T
|
XP_011540385.1:p.Ser123=
|
|
XM_011542084.1:c.369G>T
|
XP_011540386.1:p.Ser123=
|
|
XM_011542083.3:c.369G>T
|
XP_011540385.1:p.Ser123=
|
|
XM_011542084.3:c.369G>T
|
XP_011540386.1:p.Ser123=
|
|
NM_001215.4:c.357G>T
MANE Select
|
NP_001206.2:p.Ser119=
|
|
NM_001270500.2:c.357G>T
|
NP_001257429.1:p.Ser119=
|
|
NM_001270501.2:c.177G>T
|
NP_001257430.1:p.Ser59=
|
|
NM_001270502.2:c.25-1676G>T
|
NP_001257431.1:n.25-1676G>T
|
|