ENST00000215539.4:c.1431C>A
(IGFALS)
MANE Select
|
ENSP00000215539.3:p.Ala477=
|
|
ENST00000215539.3:c.1431C>A
(IGFALS)
|
ENSP00000215539.3:p.Ala477=
|
|
ENST00000415638.3:c.1545C>A
(IGFALS)
|
ENSP00000416683.3:p.Ala515=
|
|
ENST00000569769.1:c.-13+2650C>A
(SPSB3)
|
ENSP00000455098.1:n.-13+2650C>A
|
|
NM_001146006.1:c.1545C>A
(IGFALS)
|
NP_001139478.1:p.Ala515=
|
|
NM_004970.2:c.1431C>A
(IGFALS)
|
NP_004961.1:p.Ala477=
|
|
NR_027389.1:n.1485C>A
(IGFALS)
|
|
|
XM_011522476.1:c.1512C>A
(IGFALS)
|
XP_011520778.1:p.Ala504=
|
|
NM_001146006.2:c.1545C>A
(IGFALS)
|
NP_001139478.1:p.Ala515=
|
|
NM_004970.3:c.1431C>A
(IGFALS)
MANE Select
|
NP_004961.1:p.Ala477=
|
|