ENST00000209873.9:c.1574C>T
MANE Select
|
ENSP00000209873.4:p.Ser525Phe
|
|
ENST00000546562.6:n.2638C>T
|
|
|
ENST00000547238.6:n.2210C>T
|
|
|
ENST00000547520.6:n.1690C>T
|
|
|
ENST00000547757.2:c.*492C>T
|
ENSP00000448020.2:n.*492C>T
|
|
ENST00000548931.6:c.1009C>T
|
ENSP00000457518.1:p.Leu337=
|
|
ENST00000549450.6:n.1508C>T
|
|
|
ENST00000672797.1:n.2063C>T
|
|
|
ENST00000209873.8:c.1574C>T
|
ENSP00000209873.4:p.Ser525Phe
|
|
ENST00000394384.7:c.1475C>T
|
ENSP00000377908.3:p.Ser492Phe
|
|
ENST00000548931.5:c.1009C>T
|
ENSP00000457518.1:p.Leu337=
|
|
ENST00000550286.5:c.1202C>T
|
ENSP00000446885.1:p.Ser401Phe
|
|
ENST00000552876.5:n.1917C>T
|
|
|
NM_001173466.1:c.1475C>T
|
NP_001166937.1:p.Ser492Phe
|
|
NM_015665.5:c.1574C>T
|
NP_056480.1:p.Ser525Phe
|
|
XM_006719617.2:c.1589C>T
|
XP_006719680.1:p.Ser530Phe
|
|
XM_011538777.1:c.1631C>T
|
XP_011537079.1:p.Ser544Phe
|
|
XM_011538778.1:c.1616C>T
|
XP_011537080.1:p.Ser539Phe
|
|
XM_011538779.1:c.1532C>T
|
XP_011537081.1:p.Ser511Phe
|
|
XM_011538780.1:c.1517C>T
|
XP_011537082.1:p.Ser506Phe
|
|
XM_011538781.1:c.965C>T
|
XP_011537083.1:p.Ser322Phe
|
|
XM_011538778.2:c.1616C>T
|
XP_011537080.1:p.Ser539Phe
|
|
XM_011538780.2:c.1517C>T
|
XP_011537082.1:p.Ser506Phe
|
|
XR_001748875.2:n.1631C>T
|
|
|
NM_015665.6:c.1574C>T
MANE Select
|
NP_056480.1:p.Ser525Phe
|
|
NM_001173466.2:c.1475C>T
|
NP_001166937.1:p.Ser492Phe
|
|