ENST00000318471.5:c.569T>A
MANE Select
|
ENSP00000315680.3:p.Val190Glu
|
|
ENST00000541292.6:c.569T>A
|
ENSP00000441004.1:p.Val190Glu
|
|
ENST00000678002.1:c.257T>A
|
|
|
ENST00000678557.1:c.455T>A
|
ENSP00000502962.1:p.Val152Glu
|
|
ENST00000678593.1:c.574T>A
|
ENSP00000503841.1:n.574T>A
|
|
ENST00000679286.1:c.449T>A
|
ENSP00000503168.1:p.Val150Glu
|
|
ENST00000318471.4:c.569T>A
|
ENSP00000315680.3:p.Val190Glu
|
|
ENST00000541292.5:c.569T>A
|
ENSP00000441004.1:p.Val190Glu
|
|
NM_000288.3:c.569T>A
|
NP_000279.1:p.Val190Glu
|
|
XM_005267019.3:c.455T>A
|
XP_005267076.1:p.Val152Glu
|
|
XM_006715502.1:c.340-3221T>A
|
XP_006715565.1:n.340-3221T>A
|
|
XM_011535900.1:c.526+20488T>A
|
XP_011534202.1:n.526+20488T>A
|
|
XM_005267019.4:c.455T>A
|
XP_005267076.1:p.Val152Glu
|
|
XM_006715502.2:c.340-3221T>A
|
XP_006715565.1:n.340-3221T>A
|
|
XM_017010934.2:c.526+20488T>A
|
XP_016866423.1:n.526+20488T>A
|
|
NM_000288.4:c.569T>A
MANE Select
|
NP_000279.1:p.Val190Glu
|
|