ENST00000304611.13:c.1242T>G
MANE Select
|
ENSP00000303511.8:p.Ser414=
|
|
ENST00000244546.4:c.1242T>G
|
ENSP00000244546.4:p.Ser414=
|
|
ENST00000304611.12:c.1242T>G
|
ENSP00000303511.8:p.Ser414=
|
|
NM_000287.3:c.1242T>G
|
NP_000278.3:p.Ser414=
|
|
NM_001316313.1:c.978T>G
|
NP_001303242.1:p.Ser326=
|
|
NR_133009.1:n.1335T>G
|
|
|
XM_011514661.1:c.1158T>G
|
XP_011512963.1:p.Ser386=
|
|
XR_926246.1:n.1335T>G
|
|
|
XM_011514661.2:c.1158T>G
|
XP_011512963.1:p.Ser386=
|
|
XR_001743466.2:n.2316T>G
|
|
|
NM_000287.4:c.1242T>G
MANE Select
|
NP_000278.3:p.Ser414=
|
|
NM_001316313.2:c.978T>G
|
NP_001303242.1:p.Ser326=
|
|
NR_133009.2:n.1273T>G
|
|
|