ENST00000242317.9:c.1940G>A
MANE Select
|
ENSP00000242317.4:p.Gly647Asp
|
|
ENST00000242317.8:c.1940G>A
|
ENSP00000242317.4:p.Gly647Asp
|
|
ENST00000442556.1:c.329+2667G>A
|
|
|
ENST00000470169.5:c.728G>A
|
|
|
ENST00000485580.1:n.516G>A
|
|
|
ENST00000614641.4:c.1952G>A
|
ENSP00000480538.1:p.Gly651Asp
|
|
NM_001281428.1:c.1952G>A
|
NP_001268357.1:p.Gly651Asp
|
|
NM_012144.3:c.1940G>A
|
NP_036276.1:p.Gly647Asp
|
|
XM_006716758.2:c.1409G>A
|
XP_006716821.1:p.Gly470Asp
|
|
XM_011517848.1:c.1694G>A
|
XP_011516150.1:p.Gly565Asp
|
|
XM_006716758.3:c.1409G>A
|
XP_006716821.1:p.Gly470Asp
|
|
XM_011517848.2:c.1694G>A
|
XP_011516150.1:p.Gly565Asp
|
|
XM_017014625.2:c.1682G>A
|
XP_016870114.1:p.Gly561Asp
|
|
XR_002956774.1:n.2043G>A
|
|
|
NM_012144.4:c.1940G>A
MANE Select
|
NP_036276.1:p.Gly647Asp
|
|
NM_001281428.2:c.1952G>A
|
NP_001268357.1:p.Gly651Asp
|
|