ENST00000252037.5:c.588+883A>G
MANE Select
|
ENSP00000252037.4:n.588+883A>G
|
|
ENST00000648538.1:c.573+883A>G
|
ENSP00000497448.1:n.573+883A>G
|
|
ENST00000252037.4:c.588+883A>G
|
ENSP00000252037.4:n.588+883A>G
|
|
ENST00000413573.6:c.498+883A>G
|
ENSP00000394952.2:n.498+883A>G
|
|
ENST00000429879.5:c.573+898A>G
|
ENSP00000403908.1:n.573+898A>G
|
|
ENST00000431982.6:c.573+883A>G
|
ENSP00000416277.2:n.573+883A>G
|
|
ENST00000442793.5:c.453+2307A>G
|
ENSP00000402360.1:n.453+2307A>G
|
|
ENST00000445032.5:c.*667+883A>G
|
ENSP00000415891.1:n.*667+883A>G
|
|
NM_001135211.2:c.573+883A>G
|
NP_001128683.1:n.573+883A>G
|
|
NM_001281304.1:c.498+883A>G
|
NP_001268233.1:n.498+883A>G
|
|
NM_003602.4:c.588+883A>G
|
NP_003593.3:n.588+883A>G
|
|
XM_005250643.3:c.468+2307A>G
|
XP_005250700.1:n.468+2307A>G
|
|
XM_006716152.2:c.573+898A>G
|
XP_006716215.1:n.573+898A>G
|
|
XM_006716153.1:c.453+2307A>G
|
XP_006716216.1:n.453+2307A>G
|
|
XM_011516644.1:c.588+883A>G
|
XP_011514946.1:n.588+883A>G
|
|
NM_001362789.1:c.453+2307A>G
|
NP_001349718.1:n.453+2307A>G
|
|
XM_017012741.1:c.558+898A>G
|
XP_016868230.1:n.558+898A>G
|
|
XM_017012742.1:c.573+883A>G
|
XP_016868231.1:n.573+883A>G
|
|
NM_003602.5:c.588+883A>G
MANE Select
|
NP_003593.3:n.588+883A>G
|
|
NM_001135211.3:c.573+883A>G
|
NP_001128683.1:n.573+883A>G
|
|
NM_001281304.2:c.498+883A>G
|
NP_001268233.1:n.498+883A>G
|
|
NM_001362789.2:c.453+2307A>G
|
NP_001349718.1:n.453+2307A>G
|
|