ENST00000212015.11:c.513A>T
MANE Select
|
ENSP00000212015.6:p.Ala171=
|
|
ENST00000212015.10:c.513A>T
|
ENSP00000212015.6:p.Ala171=
|
|
ENST00000432464.5:c.-131A>T
|
ENSP00000409208.1:n.-131A>T
|
|
ENST00000473922.1:n.299A>T
|
|
|
ENST00000497639.5:n.302A>T
|
|
|
NM_001142498.1:c.-131A>T
|
NP_001135970.1:n.-131A>T
|
|
NM_012238.4:c.513A>T
|
NP_036370.2:p.Ala171=
|
|
XM_006717737.2:c.513A>T
|
XP_006717800.1:p.Ala171=
|
|
XM_011539561.1:c.-64A>T
|
XP_011537863.1:n.-64A>T
|
|
NM_012238.5:c.513A>T
MANE Select
|
NP_036370.2:p.Ala171=
|
|
NM_001142498.2:c.-131A>T
|
NP_001135970.1:n.-131A>T
|
|