ENST00000449291.7:c.1590C>T
MANE Select
|
ENSP00000401508.2:p.Asn530=
|
|
ENST00000340490.7:c.1675C>T
|
ENSP00000341136.3:p.Gln559Ter
|
|
ENST00000426292.7:c.1551C>T
|
ENSP00000390949.3:p.Asn517=
|
|
ENST00000435154.7:c.*299C>T
|
ENSP00000405670.3:n.*299C>T
|
|
ENST00000449291.6:c.1590C>T
|
ENSP00000401508.2:p.Asn530=
|
|
ENST00000460623.5:c.614C>T
|
|
|
ENST00000464332.5:n.1134C>T
|
|
|
ENST00000498076.5:n.369C>T
|
|
|
ENST00000529179.1:n.374C>T
|
|
|
NM_001286829.1:c.1551C>T
|
NP_001273758.1:p.Asn517=
|
|
NM_145201.5:c.1590C>T
|
NP_660202.3:p.Asn530=
|
|
XM_011517377.1:c.1327C>T
|
XP_011515679.1:p.Gln443Ter
|
|
NM_001363145.1:c.1509C>T
|
NP_001350074.1:p.Asn503=
|
|
NM_001363146.1:c.906C>T
|
NP_001350075.1:p.Asn302=
|
|
XM_017013975.2:c.1894C>T
|
XP_016869464.1:p.Gln632Ter
|
|
XM_017013976.2:c.1809C>T
|
XP_016869465.1:p.Asn603=
|
|
XM_017013977.2:c.1594C>T
|
XP_016869466.1:p.Gln532Ter
|
|
XM_017013978.2:c.1546C>T
|
XP_016869467.1:p.Gln516Ter
|
|
XM_017013979.2:c.991C>T
|
XP_016869468.1:p.Gln331Ter
|
|
XM_024447332.1:c.964C>T
|
XP_024303100.1:p.Gln322Ter
|
|
XM_024447333.1:c.910C>T
|
XP_024303101.1:p.Gln304Ter
|
|
NM_145201.6:c.1590C>T
MANE Select
|
NP_660202.3:p.Asn530=
|
|
NM_001286829.2:c.1551C>T
|
NP_001273758.1:p.Asn517=
|
|