ENST00000456935.7:c.603T>G
MANE Select
|
ENSP00000395473.2:p.Ser201=
|
|
ENST00000221363.8:c.603T>G
|
ENSP00000221363.4:p.Ser201=
|
|
ENST00000456935.6:c.603T>G
|
ENSP00000395473.2:p.Ser201=
|
|
ENST00000466794.5:n.585T>G
|
|
|
ENST00000486847.2:c.333+533T>G
|
ENSP00000470174.1:n.333+533T>G
|
|
ENST00000596512.5:n.541T>G
|
|
|
NM_000528.3:c.603T>G
|
NP_000519.2:p.Ser201=
|
|
NM_001173498.1:c.603T>G
|
NP_001166969.1:p.Ser201=
|
|
XM_005259913.1:c.603T>G
|
XP_005259970.1:p.Ser201=
|
|
XM_005259913.2:c.603T>G
|
XP_005259970.1:p.Ser201=
|
|
XM_024451518.1:c.-416T>G
|
XP_024307286.1:n.-416T>G
|
|
NM_000528.4:c.603T>G
MANE Select
|
NP_000519.2:p.Ser201=
|
|
NM_001173498.2:c.603T>G
|
NP_001166969.1:p.Ser201=
|
|