ENST00000409418.9:c.705+24302A>G
MANE Select
|
ENSP00000386722.4:n.705+24302A>G
|
|
ENST00000311172.11:c.537+24302A>G
|
ENSP00000308978.7:n.537+24302A>G
|
|
ENST00000409314.5:c.705+24302A>G
|
ENSP00000386987.1:n.705+24302A>G
|
|
ENST00000409418.8:c.705+24302A>G
|
ENSP00000386722.4:n.705+24302A>G
|
|
ENST00000409853.5:c.537+24302A>G
|
ENSP00000386314.1:n.537+24302A>G
|
|
ENST00000458644.6:c.225+24302A>G
|
ENSP00000402972.2:n.225+24302A>G
|
|
NM_014824.2:c.705+24302A>G
|
NP_055639.2:n.705+24302A>G
|
|
XM_011545409.1:c.642+24302A>G
|
XP_011543711.1:n.642+24302A>G
|
|
XM_011545410.1:c.630+24302A>G
|
XP_011543712.1:n.630+24302A>G
|
|
XM_011545411.1:c.471+24302A>G
|
XP_011543713.1:n.471+24302A>G
|
|
XM_011545412.1:c.705+24302A>G
|
XP_011543714.1:n.705+24302A>G
|
|
XM_011545410.2:c.630+24302A>G
|
XP_011543712.1:n.630+24302A>G
|
|
XM_017018632.1:c.642+24302A>G
|
XP_016874121.1:n.642+24302A>G
|
|
XR_001748055.1:n.1510+24302A>G
|
|
|
NM_014824.3:c.705+24302A>G
MANE Select
|
NP_055639.2:n.705+24302A>G
|
|