ENST00000431087.2:c.183+17569T>G
|
ENSP00000395957.2:n.183+17569T>G
|
|
ENST00000697752.1:c.324+17569T>G
|
ENSP00000513431.1:n.324+17569T>G
|
|
ENST00000315872.11:c.324+17569T>G
MANE Select
|
ENSP00000317985.6:n.324+17569T>G
|
|
ENST00000261535.7:c.324+17569T>G
|
ENSP00000261535.3:n.324+17569T>G
|
|
ENST00000315872.10:c.324+17569T>G
|
ENSP00000317985.6:n.324+17569T>G
|
|
ENST00000431087.1:c.66+17569T>G
|
ENSP00000395957.1:n.66+17569T>G
|
|
ENST00000462366.1:n.346+17569T>G
|
|
|
ENST00000616279.4:c.-1732+17569T>G
|
ENSP00000481789.1:n.-1732+17569T>G
|
|
NM_004850.3:c.324+17569T>G
|
NP_004841.2:n.324+17569T>G
|
|
XM_005246190.3:c.324+17569T>G
|
XP_005246247.1:n.324+17569T>G
|
|
XM_011510417.1:c.66+17569T>G
|
XP_011508719.1:n.66+17569T>G
|
|
NM_001321643.1:c.66+17569T>G
|
NP_001308572.1:n.66+17569T>G
|
|
NM_004850.4:c.324+17569T>G
|
NP_004841.2:n.324+17569T>G
|
|
XM_011510417.2:c.66+17569T>G
|
XP_011508719.1:n.66+17569T>G
|
|
XM_017005378.2:c.324+17569T>G
|
XP_016860867.1:n.324+17569T>G
|
|
XM_017005379.2:c.66+17569T>G
|
XP_016860868.1:n.66+17569T>G
|
|
NM_004850.5:c.324+17569T>G
MANE Select
|
NP_004841.2:n.324+17569T>G
|
|
NM_001321643.2:c.66+17569T>G
|
NP_001308572.1:n.66+17569T>G
|
|