ENST00000209873.9:c.1501G>C
MANE Select
|
ENSP00000209873.4:p.Ala501Pro
|
|
ENST00000546562.6:n.2565G>C
|
|
|
ENST00000547238.6:n.2137G>C
|
|
|
ENST00000547520.6:n.1617G>C
|
|
|
ENST00000547757.2:c.*419G>C
|
ENSP00000448020.2:n.*419G>C
|
|
ENST00000548931.6:c.936G>C
|
ENSP00000457518.1:p.Gly312=
|
|
ENST00000549450.6:n.1435G>C
|
|
|
ENST00000672797.1:n.1990G>C
|
|
|
ENST00000209873.8:c.1501G>C
|
ENSP00000209873.4:p.Ala501Pro
|
|
ENST00000394384.7:c.1402G>C
|
ENSP00000377908.3:p.Ala468Pro
|
|
ENST00000548931.5:c.936G>C
|
ENSP00000457518.1:p.Gly312=
|
|
ENST00000550286.5:c.1129G>C
|
ENSP00000446885.1:p.Ala377Pro
|
|
ENST00000552876.5:n.1844G>C
|
|
|
NM_001173466.1:c.1402G>C
|
NP_001166937.1:p.Ala468Pro
|
|
NM_015665.5:c.1501G>C
|
NP_056480.1:p.Ala501Pro
|
|
XM_006719617.2:c.1516G>C
|
XP_006719680.1:p.Ala506Pro
|
|
XM_011538777.1:c.1558G>C
|
XP_011537079.1:p.Ala520Pro
|
|
XM_011538778.1:c.1543G>C
|
XP_011537080.1:p.Ala515Pro
|
|
XM_011538779.1:c.1459G>C
|
XP_011537081.1:p.Ala487Pro
|
|
XM_011538780.1:c.1444G>C
|
XP_011537082.1:p.Ala482Pro
|
|
XM_011538781.1:c.892G>C
|
XP_011537083.1:p.Ala298Pro
|
|
XM_011538778.2:c.1543G>C
|
XP_011537080.1:p.Ala515Pro
|
|
XM_011538780.2:c.1444G>C
|
XP_011537082.1:p.Ala482Pro
|
|
XR_001748875.2:n.1558G>C
|
|
|
NM_015665.6:c.1501G>C
MANE Select
|
NP_056480.1:p.Ala501Pro
|
|
NM_001173466.2:c.1402G>C
|
NP_001166937.1:p.Ala468Pro
|
|