ENST00000265598.8:c.888+10G>A
MANE Select
|
ENSP00000265598.3:n.888+10G>A
|
|
ENST00000265598.7:c.888+10G>A
|
ENSP00000265598.3:n.888+10G>A
|
|
ENST00000466939.1:c.816+10G>A
|
ENSP00000418912.1:n.816+10G>A
|
|
NM_014398.3:c.888+10G>A
|
NP_055213.2:n.888+10G>A
|
|
XM_005247360.3:c.888+10G>A
|
XP_005247417.1:n.888+10G>A
|
|
XM_006713586.2:c.816+10G>A
|
XP_006713649.1:n.816+10G>A
|
|
XM_011512688.1:c.888+10G>A
|
XP_011510990.1:n.888+10G>A
|
|
XR_924123.1:n.948+10G>A
|
|
|
XR_924124.1:n.948+10G>A
|
|
|
XM_005247360.5:c.888+10G>A
|
XP_005247417.1:n.888+10G>A
|
|
XM_006713586.3:c.816+10G>A
|
XP_006713649.1:n.816+10G>A
|
|
XM_011512688.2:c.888+10G>A
|
XP_011510990.1:n.888+10G>A
|
|
XM_024453453.1:c.816+10G>A
|
XP_024309221.1:n.816+10G>A
|
|
NM_014398.4:c.888+10G>A
MANE Select
|
NP_055213.2:n.888+10G>A
|
|