ENST00000327475.11:c.4609C>T
MANE Select
|
ENSP00000333363.7:p.Arg1537Cys
|
|
ENST00000327475.10:c.4609C>T
|
ENSP00000333363.7:p.Arg1537Cys
|
|
ENST00000359357.7:c.3958C>T
|
ENSP00000352312.3:p.Arg1320Cys
|
|
ENST00000449981.6:c.4609C>T
|
ENSP00000415331.2:p.Arg1537Cys
|
|
NM_001206927.1:c.4609C>T
|
NP_001193856.1:p.Arg1537Cys
|
|
XM_011514318.1:c.4546C>T
|
XP_011512620.1:p.Arg1516Cys
|
|
XM_011514319.1:c.4609C>T
|
XP_011512621.1:p.Arg1537Cys
|
|
XM_011514320.1:c.4372C>T
|
XP_011512622.1:p.Arg1458Cys
|
|
XM_011514321.1:c.3958C>T
|
XP_011512623.1:p.Arg1320Cys
|
|
XM_011514322.1:c.4609C>T
|
XP_011512624.1:p.Arg1537Cys
|
|
XR_926078.1:n.4726C>T
|
|
|
NM_001371.3:c.3958C>T
|
NP_001362.2:p.Arg1320Cys
|
|
XM_011514318.2:c.4546C>T
|
XP_011512620.1:p.Arg1516Cys
|
|
XM_011514319.2:c.4609C>T
|
XP_011512621.1:p.Arg1537Cys
|
|
XM_011514320.2:c.4372C>T
|
XP_011512622.1:p.Arg1458Cys
|
|
XM_017010325.1:c.4609C>T
|
XP_016865814.1:p.Arg1537Cys
|
|
XM_017010326.1:c.4609C>T
|
XP_016865815.1:p.Arg1537Cys
|
|
XM_017010327.1:c.4609C>T
|
XP_016865816.1:p.Arg1537Cys
|
|
XR_001743188.1:n.4730C>T
|
|
|
XR_926078.2:n.4729C>T
|
|
|
NM_001206927.2:c.4609C>T
MANE Select
|
NP_001193856.1:p.Arg1537Cys
|
|
NM_001371.4:c.3958C>T
|
NP_001362.2:p.Arg1320Cys
|
|