ENST00000444124.7:c.-29+4225T>G
MANE Select
|
ENSP00000403644.2:n.-29+4225T>G
|
|
ENST00000420203.1:c.-29+2935T>G
|
ENSP00000408626.1:n.-29+2935T>G
|
|
ENST00000444124.6:c.-29+4225T>G
|
ENSP00000403644.2:n.-29+4225T>G
|
|
ENST00000615193.4:c.-75T>G
|
ENSP00000484104.1:n.-75T>G
|
|
ENST00000617822.4:c.-75T>G
|
ENSP00000478385.1:n.-75T>G
|
|
ENST00000622873.4:c.-75T>G
|
ENSP00000479110.1:n.-75T>G
|
|
NM_000790.3:c.-75T>G
|
NP_000781.1:n.-75T>G
|
|
NM_001082971.1:c.-29+4225T>G
|
NP_001076440.1:n.-29+4225T>G
|
|
NM_001242886.1:c.-75T>G
|
NP_001229815.1:n.-75T>G
|
|
NM_001242887.1:c.-75T>G
|
NP_001229816.1:n.-75T>G
|
|
NM_001242888.1:c.-75T>G
|
NP_001229817.1:n.-75T>G
|
|
NM_001242889.1:c.-75T>G
|
NP_001229818.1:n.-75T>G
|
|
NM_001242890.1:c.-75T>G
|
NP_001229819.1:n.-75T>G
|
|
XM_005271745.3:c.-29+4225T>G
|
XP_005271802.1:n.-29+4225T>G
|
|
XM_005271745.4:c.-29+4225T>G
|
XP_005271802.1:n.-29+4225T>G
|
|
NM_001082971.2:c.-29+4225T>G
MANE Select
|
NP_001076440.2:n.-29+4225T>G
|
|
NM_000790.4:c.-75T>G
|
NP_000781.2:n.-75T>G
|
|
NM_001242888.2:c.-75T>G
|
NP_001229817.2:n.-75T>G
|
|
NM_001242890.2:c.-75T>G
|
NP_001229819.2:n.-75T>G
|
|
NM_001242886.2:c.-75T>G
|
NP_001229815.2:n.-75T>G
|
|
NM_001242887.2:c.-75T>G
|
NP_001229816.2:n.-75T>G
|
|
NM_001242889.2:c.-75T>G
|
NP_001229818.2:n.-75T>G
|
|